(E)-2-(5-Fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)-5-(phenyldiazenyl)pyrimidine-4,6-diamine: An In-Depth Review

Historical Development

Chemists have long wrestled with complex heterocycles, piecing together building blocks to create molecules with useful properties. The journey toward synthesizing structures like (E)-2-(5-Fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)-5-(phenyldiazenyl)pyrimidine-4,6-diamine traces back to the drive for new drugs targeting tough medical problems. Modifying pyrimidine and pyrazolopyridine scaffolds has often unlocked new doors for antiviral, antibacterial, and anticancer research. Chemists found that combining these motifs, and working fluorine into the structure, made molecules with improved metabolic stability and stronger binding to biological targets. The inclusion of diazenyl linkages brought color and electronic diversity. Pushback from challenging reaction conditions, low solubility, and tough purification steps didn’t stop the molecular architects. Every step forward in accessible methods for making such compounds sparked new collaborations between academia and pharmaceutical labs.

Product Overview

Looking at this chemical, you’re faced with a small molecule carrying a big toolkit. The blend of fluoroarene, pyrazolo[3,4-b]pyridine, and diazenyl-linked pyrimidine means it can show up on the bench as a solid with a striking color. Many labs pursue fluorinated heterocycles because they stick around longer in the body and sometimes break through resistance seen in bacteria or tumor cells. In practice, this compound shows up in screening panels, among colorimetric sensors, and as a stepping stone in medicinal chemistry. Researchers holding a bottle of this substance see a compound with sharp lines on NMR and a clear UV-vis feature — not just another white powder drawn from the shelf.

Physical & Chemical Properties

This molecule packs in several aromatic systems and features electron-withdrawing fluorine atoms at strategic positions. Practically speaking, this increases its lipophilicity and thermal stability. The presence of an azo group and diamine sites stretches the electron cloud, adding to its chromophore properties — you often spot yellow-to-red crystals depending on the polymorph and crystal habit. The melting point rises above many simple heterocycles, usually reflecting tougher intermolecular forces. It tends not to dissolve well in pure water, but you’ll see reasonable solubility in polar aprotic solvents like DMSO or DMF. In the flask, you’ll notice the distinctive color, and by TLC or HPLC, it gives a strong, trackable spot. This speaks to the usability for both analytics and downstream reactions.

Technical Specifications & Labeling

On the bottle, you’d find data like purity percentages, suggested storage temperature (often under inert gas, away from light, at -20°C), and batch reference numbers. More rigorous suppliers print out full spectra: HPLC assessment with retention time, carbon and proton NMR shifts, and sometimes a powder X-ray diffractogram. These details matter because impurities, light, and moisture will change the compound over weeks. Labels carry GHS hazard pictograms warning about possible toxicity or irritation, and the MSDS offers point-by-point advice on handling spills or accidental exposure. Every researcher depends on these facts to avoid running reactions with degraded or contaminated chemicals.

Preparation Method

Synthesizing this target means coaxing several reactive partners to work together. In most routes, chemists start by putting together the pyrazolo[3,4-b]pyridine core, either with cyclization of hydrazines and β-dicarbonyls or through a sequence of condensation and oxidative closure. The fluorobenzyl group usually gets attached through nucleophilic aromatic substitution or, more elegantly, via transition-metal-catalyzed cross-coupling. Introducing the diazenyl functionality follows classic azo coupling: create a diazonium salt from an aromatic amine under cold conditions, then react with the pyrimidine partner in basic solution. Final stages clean up the mixture with flash chromatography and crystallization. At each step, yields depend on solvent choice, temperature, and the skill of the chemist. The process feels like guiding a relay team across a field littered with side reactions, each step requiring tuning and adjustment.

Chemical Reactions & Modifications

The molecule lends itself to further change. Chemists can tweak the diazenyl bridge’s electronics, introduce other substituents on the aromatic systems, or use the amine groups for acylation and alkylation. The fluoro groups hold steady under most reaction conditions, giving stability against harsh reagents. Over the years, teams have explored catalytic hydrogenation to cleave the azo linkage, turning colorful compounds clear and revealing new pharmacophores in the process. The core paves a path for conjugation to polymers, the addition of reporter groups for imaging, or attachment to larger biomolecules for targeted delivery. Every new variant undergoes a fresh round of spectral and functional testing, hinting at bioactivity or new material uses.

Synonyms & Product Names

Depending on the lab or database, you might encounter alternative names reflecting the structure: “fluorobenzyl-pyrazolopyridinyl diazenyl pyrimidinediamine” or specific abbreviated handles in screening libraries. CAS numbers help ensure clarity during procurement, and suppliers may tag products by batch or code names for tracking.

Safety & Operational Standards

Working with this compound, you learn to respect its hazard labels. The fluorinated rings and diazenyl group hint at toxicity, so the standard gear includes gloves, goggles, and use inside a well-ventilated fume hood. Experience teaches that accidents don’t offer second chances: I once saw a splash from an azo compound burn a hole in latex gloves. Clean handling and regular surface wipes keep residues from spreading. Lab protocols require spill kits with absorbent granules and instructions for local solvent disposal rules, since water washing rarely does the trick. Teams brief new users, stressing the need to avoid inhaling dust and the importance of cleanup routines, because even micrograms of this stuff can show up in wipe-tests days later.

Application Area

Researchers chase targets like this in the search for new drugs and advanced materials. The combination of heterocycles and fluorine pushes molecules into use as kinase inhibitors, imaging agents, and chemosensors. Some labs focus on the compound’s ability to disrupt bacterial DNA gyrase or block mutant tyrosine kinases in cancer studies. A project I worked on screened similar molecules against multidrug-resistant E. coli — the fluorinated group resisted metabolic breakdown, hinting at longer-lasting effects. Material science teams value the stable chromophores for ink ingredients or as sensors responding to shifts in pH, ions, or light. Patents from major pharma companies show up with these motifs, drawn by the fine blend of reactivity and resilience.

Research & Development

Much of the excitement comes from iterative research. Academic groups map out structure-activity relationships, swapping in halogens, tweaking linkers, or trying ring expansions — all to dial in activity or selectivity. Big data methods and high-throughput screens speed up the work. Collaboration across chemistry, biology, and pharma means discoveries flow from test tubes to in vivo trials more quickly. Many green chemistry projects now look for cleaner ways to build these molecules, reducing reliance on heavy metals or hazardous solvents. In some partnerships, I saw early NMR data turn into leads within months, new knowledge built on past breakthroughs. The pace quickens as machine learning identifies promising variants before we’ve even finished the synthesis.

Toxicity Research

No one ignores safety. Teams have run in vitro cytotoxicity tests on liver cell lines, checking for dose-dependent effects and long-lasting residues. The diazenyl group can sometimes break down, forming aromatic amines that risk causing DNA mutations or enzyme disruption. Some studies track breakdown products across simulated digestive systems, looking for unwanted bioaccumulation. Animal studies, though increasingly replaced by organ-on-chip models, probe for signs of organ stress. I’ve worked on analytical projects checking wastewater for persistent breakdown products — a reminder that what goes down the drain could turn up later in waterways unless we’re careful.

Future Prospects

With global disease patterns changing and antibiotic resistance climbing, researchers see room for more exploration here. Advanced syntheses automate steps, making new analogs more accessible. AI and computational chemistry push us to predict toxicity and activity before hitting the lab. We also see pushes toward more biodegradable or less-persistent variants, to keep pace with environmental concerns. Drug pipelines run leaner, but a molecule with this much complexity will keep finding niches in both healthcare and advanced technology. Students entering the field take up older literature, thinking about new uses for compounds their mentors only dreamed about. This compound stands as a testament to the value of multidisciplinary teamwork and the simple determination to make something new, even with all the hurdles.



What is the primary use or application of (E)-2-(5-Fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)-5-(phenyldiazenyl)pyrimidine-4,6-diamine?

Stepping Into the World of Modern Kinase Inhibitors

Walk into any pharmaceutical R&D lab and ask about kinase inhibitors. Nearly all drug discovery teams have stories about painstaking searches for the right molecule to target cancer or rare autoimmune diseases. Chemists have seen Pyrazolopyridine-based compounds take center stage, and in the list of newer kinase inhibitors, (E)-2-(5-Fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)-5-(phenyldiazenyl)pyrimidine-4,6-diamine often comes up. What does this tongue-twister of a chemical actually do? The heart of the answer sits in targeted therapy for complex illnesses.

Targeting Cancer With Precision

Cancer research in the last couple of decades has moved away from the sledgehammer approach of old chemotherapy drugs. Now, the focus lands on molecules that target specific proteins involved in cancer cell growth and survival. The structure of this pyrimidine-diamine derivative lets it slip into the ATP binding pocket of certain kinases—a class of enzymes central to signal transduction in cells. Disrupting these pathways can stop runaway cell division in its tracks. This compound, by virtue of that fluorinated backbone, stands out among kinase inhibitors for its selectivity and ability to dodge off-target interactions that can cause nasty side effects. Studies show that these molecules are being explored in preclinical models of leukemia and certain solid tumors, especially those involving mutations in the ALK and ROS1 pathways.

Pushing Beyond Oncology: Potential for Autoimmune Disease

Cancer isn’t the only field benefiting from focused kinase regulation. Many autoimmune diseases trace back to misguided cellular signaling, particularly in T-cells and B-cells. Scientists see hope in this compound’s structural class as a way to calm down overactive immune systems without shutting them down completely. I have witnessed firsthand the relief felt by families after seeing the change that a targeted therapy can bring, compared to broad immunosuppressants with long-term risks. Early research points to the possibility of addressing rare autoimmune syndromes—like some types of inflammatory bowel disease or lupus—where traditional therapies leave patients with few options.

Synthesis and Scalability: Practical Challenges

Many promising molecules end up as footnotes in research journals because they’re a nightmare to manufacture or purify. Here lies another reason why the industry keeps its eye on this class of compounds. The key intermediates in the synthesis process are relatively robust, with established routes that chemists can follow at both bench and pilot scale. This reliability opens the door to efficient optimization, enabling rapid movement from the lab to real-world clinical supply. The presence of fluoro groups, while making the synthesis a bit tricky, also gives the molecule metabolic stability, which could mean fewer breakdown products in patients and a longer half-life.

Room for Cautious Optimism

As these developments unfold, it’s important to remember that drug discovery never guarantees clinical success. Off-target effects may arise down the line. Resistance mechanisms can still develop after months or years of therapy. The big test arrives during multi-site clinical trials, with real people and complex histories. For every promising compound, hundreds never cross the finish line. Still, with sharp selectivity, manageable chemistry, and broad potential across serious illnesses, this molecule joins a growing list of tools turning personalized medicine from hope into reality.

What are the storage conditions required for this compound?

Getting Storage Right Keeps People and Compounds Safe

Some chemicals change in a blink if handled poorly. Picture a bag of rice: leave it in the sun and bugs, humidity, or mold ruin it. Chemicals have quirks, too. They break down, change color, form crystals, or even turn dangerous with just a bit of heat or dampness. Reliable storage doesn’t just tick a box on a safety checklist—it prevents fires, lost money, and ruined experiments.

Temperature Fluctuations: The Enemy Nobody Sees

Leaving certain compounds in a hot room leads to slow disasters. Some degrade. Some containers swell and burst. I’ve seen colleagues lose months of work because a fridge compressor failed over a weekend. Data from the US Chemical Safety Board show that improper storage temperatures frequently appear in accident reports, especially with volatile or unstable substances. Keeping a stable temperature, either at room temperature, refrigerated, or even frozen, often spells the difference between a successful batch and a hazardous cleanup.

Humidity and Air: More Trouble Than Most Think

Moisture in the air sneaks into loose lids and porous seals. Powders clump and solids liquefy. To avoid messes, people use desiccators, sometimes with color-changing silica gel to know when to switch it out. Open windows or sloppy habits bring in unexpected water. Even things that look stable can react with carbon dioxide, turning a potassium hydroxide pellet into a useless lump of carbonate. Almost every lab uses a tight-sealing system or stores compounds under nitrogen or argon to keep the air out.

Sunlight and Light Exposure: The Fading Factor

Some chemicals change or break down in regular sunlight. I remember opening a bottle of photosensitive dye after weeks in a sunlit cabinet, only to find it colorless. Protection is easy—a brown glass bottle or a dark drawer. It pays off over time, especially for expensive chemicals. Pharmacies and manufacturers spend on coated bottles and automatic blinds to shield delicate materials.

Clutter and Cross Contamination: Hidden Risks

Overstuffed shelves stack risks. When strong acids crowd next to bases, or oxidizers mix with flammable liquids, accidents happen. The CDC has linked chemical mishaps to poor organization in storage rooms more than once. Clear labeling, separate cabinets, and reliable logbooks help everyone avoid mistakes—especially in busy places or when staff turnover looms. I’ve seen the relief on a tech’s face when a color-coded shelf points straight to the right bottle.

What Fixes the Storage Problem?

Training everyone, not just the safety officer, matters most. Eye-level reminders and posters beat email warnings. Investing in the right fridge, using humidity indicators, and setting strict shelf rules cost far less than an emergency room visit. Plenty of places post safety data online for free, so nobody should guess storage rules. At the end of the day, careful storage protects people first, and keeps science, medicine, and industry moving forward without headaches.

What is the chemical purity and how is it verified?

The Basics of Chemical Purity

Think about the salt on your kitchen table. Most of it is sodium chloride, but even table salt isn’t pure—there’s a pinch of iodine, some silica to keep it free-flowing, and maybe trace minerals depending on the brand. Chemical purity reflects how much of a sample is actually the chemical you want. In science and industry, the rest gets referred to as impurities, and even tiny amounts can throw off experiments, manufacturing processes, or medication safety.

Why Purity Matters

Purity matters more than some might suspect. In the lab, a small impurity in a reagent can mean the wrong results, wasted time, or a ruined experiment. In medicine, a contaminated compound can put lives at risk. In electronics, pure materials help make smaller, faster, and more reliable devices. For food production, purity supports both taste and safety. Some folks picture scientists as sticklers, but those decimal points in purity percentages affect real outcomes and personal health.

How We Spot Impurities

Verifying purity draws on both tradition and high-tech tools. When I worked in an academic lab, we'd lean on classic tests—melting point checks, color changes, or simple solubility trials. If something melted at 150°C instead of 153°C, you knew there was a problem. These basic methods still help, but they can only take you so far.

For the precision needed by today’s manufacturers and researchers, we use a modern set of eyes: analytical machines. Mass spectrometry reads out the chemical composition down to millionths of a gram. Chromatography separates the different bits in a mixture, letting us measure exactly what’s in there. Nuclear magnetic resonance, or NMR, shines a light on molecular structure, helping rule out hidden surprises. Even these sophisticated methods need trained operators to read the results, set standards, and double-check things when results look off.

The Limits and Reality of Purity

Absolute purity might sound ideal, but it’s just not realistic for most real-world chemicals. Total absence of contaminants costs an enormous amount of effort and money. So, chemists set acceptable limits depending on use. Pharmaceutical standards run tight: the United States Pharmacopeia or the European equivalent puts hard rules on how much impurity can show up in a drug. Electronics makers seek parts-per-billion purity for silicon wafers, because even a speck of the wrong element can turn a chip into junk.

Not everything requires pharmaceutical attention. In agriculture, fertilizer only needs enough purity to avoid harming plants or clogging machinery. Paints, cleaners, and industrial solvents have standards, but those focus more on performance than scientific perfection. What matters is matching the level of purity to the risk or reward involved. If you’re brewing up a new cancer drug, you aim high; if you’re cleaning the garage, good enough becomes just that.

Staying Trustworthy and Transparent

Verifying purity means more than just testing. It takes keeping strong records, having outside experts certify results, and tracking batches from start to finish. Trust comes from transparency—being honest about risks, admitting limitations, and updating practices as new findings emerge. Professionals pass audits, publish methods, and keep up with changing regulations to earn and maintain that trust.

Finding Solutions and Building Better Habits

Improving chemical purity across the board won’t happen in a vacuum. Companies can invest in cleaner production, reduce cross-contamination in facilities, and share best practices across industries. Everyday users can check labels, ask suppliers questions, and understand what “food grade” or “lab grade” really means. Government agencies ought to keep raising awareness and enforcing sensible standards, because safety is not just a technical problem—it’s a public responsibility.

Are there any known safety or handling precautions for this product?

Why Messing Around with Safety Isn’t Worth It

There’s a good reason parents teach kids to “read the label.” Getting careless with a product, whether it’s a cleaning spray or a battery, can turn a regular day sideways. I’ve learned the hard way that hurrying through directions usually spells trouble. Once, I splashed a household cleaner on my face because I used a bottle with a cracked cap—straight to burning eyes and a reminder that corners only look good when they’re not being cut.

Understanding What’s Really at Stake

People need to know what they’re picking up and bringing home. Skin can react to one product, lungs to another. Chemical burns, breathing trouble, and allergies pop up all the time in emergency rooms. In factories, you see workers reaching for gloves and goggles for a reason. According to the CDC, accidental poisoning lands over two million Americans in ERs every year, and about half of those cases involve cleaning agents or personal care products. That tells me the danger isn’t exaggerated.

The Small Print Tells a Bigger Story

Most folks ignore fine print tucked on bottles and boxes. Skipping those words means you miss out on basics, like “store away from sunlight,” “don’t mix with bleach,” or “keep out of reach of kids.” Some chemicals react with iron, others go off-gas if you let lids hang loose. A garage filled with old, half-empty containers acts like a chemistry set with bad intentions. Over my years helping neighbors clean out sheds, I’ve seen people hoarding paint thinners next to fertilizer—one spark could cost a house.

The Chain Reaction of Carelessness

Spills rarely stay in one spot. A drip on the kitchen floor can lead to slips. Leaks work through cardboard boxes, damage furniture, and poison pets sniffing around. I remember a case where a friend’s cat fell ill after chewing on a rag that wiped up an insecticide spill. The mess grew from an ignored warning into a hefty vet bill and a week of worry.

Steps That Make a Difference

Storing chemicals on high shelves, away from food, buys a lot of peace of mind. Choosing locked cabinets over open ones makes life easier when kids roam the house. Labels featuring the words “danger,” “warning,” or “caution” flag the need for care. Simple steps like wearing gloves, working in a breeze-filled area, and never mixing random bottles keep a lot of trouble away.

Disposing of unwanted or expired products with scheduled community hazardous waste days keeps toxic stuff out of landfills and water. There’s no victory in pouring paint thinner down the drain or tossing batteries in regular trash. I once joined a local drop-off day and saw barrels worth of old pesticide bottles—proof that hidden stockpiles live everywhere and need a safe exit.

Moving from Warnings to Habits

Old habits die hard, but getting educated and sharing what’s learned keeps families and neighbors safe. Good safety starts at home, but it doesn’t stay there. Every product tells a story on its label, if you’re willing to listen. Common sense and a few extra seconds spent reading make all the difference between a close call and smooth sailing.

What is the molecular weight and chemical structure of this compound?

Getting Down to the Basics

Every compound tells a story through its molecular weight and chemical structure. The numbers on the periodic table aren’t just for show. They help us piece together not just what a substance is, but what it might do, how it moves through our bodies, and the way it interacts with the environment around us.

Deep Dive into Molecular Weight

Teachers used to hand me a periodic table and say, “Add up the values, that’s your molecular weight.” I never understood why this number mattered so much until doses of medicine started making sense. Molecular weight gives us real-deal information about how much of something ends up in a tablet, or how effective a drug delivery system could be. Take aspirin. Its molecular weight sits at about 180 grams per mole. This number tells you how much aspirin you’d need to measure to make sure you’ve got a mole, but it also lets researchers judge how easily the drug makes its way through cells. Low molecular weight often means easy passage, and higher weights might slow things down or keep them out entirely.

Chemical Structure Reveals the Tricks

Imagine looking at a puzzle and trying to guess what picture you’ll end up with. That’s chemical structure — a roadmap, full of twists and connections. Consider glucose and galactose: almost identical structures, turned just a bit differently, and suddenly your body handles them in unique ways. Even minor tweaks, such as sticking on an extra group or rearranging atoms, can spell the difference between a life-saving medicine and a toxic hazard.

Real-World Impact on Health and Industry

Walk into any pharmacy and you see how much rides on a compound’s structure. Penicillin works because of a tiny beta-lactam ring in its core. Swap that ring for something else, and bacteria shrug off the drug. This is not just academic curiosity. The opioid crisis, for instance, spiraled partly because small chemical changes create stronger or more dangerous compounds, sometimes legal until regulators catch up. Structure isn’t just a diagram on a page. It carries the weight of consequences, good or bad.

Trust Through Transparency

I’ve always believed that trust comes from showing your work. Reliable science means sharing molecular weights and structures openly. Publishing these details helps scientists double-check results, formulate safe products, and keep counterfeit drugs off the shelves. Without that kind of transparency, everyone is left guessing — and mistakes become more likely.

Keeping Science Accountable

Easy access to chemical details makes all the difference. Databases like PubChem or the Chemical Abstracts Service let researchers and the public find these values without much fuss. Regulators, manufacturers, and even consumers can trace where a compound came from and what risks it might carry. I once tracked the contamination source in a personal care product because its molecular weight didn’t match what the label claimed. Catching that early might save lives.

How to Bring Solutions Forward

Accuracy needs commitment at every step. Scientists check their measurements with tried-and-true lab work. Industries invest in better analytic equipment so mistakes slip through less often. Publishing full chemical structures alongside molecular weights keeps the whole process honest and raises the bar for the next discovery. Education can start earlier, too — more hands-on chemistry in classrooms means a sharper public eye in the future.

(E)-2-(5-Fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)-5-(phenyldiazenyl)pyrimidine-4,6-diamine
(E)-2-(5-Fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)-5-(phenyldiazenyl)pyrimidine-4,6-diamine
(E)-2-(5-Fluoro-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl)-5-(phenyldiazenyl)pyrimidine-4,6-diamine