5-Bromo-2-cyano-3-fluoropyridine

    • Product Name: 5-Bromo-2-cyano-3-fluoropyridine
    • Chemical Name (IUPAC): 5-bromo-3-fluoro-2-pyridinecarbonitrile
    • CAS No.: 1019875-49-2
    • Chemical Formula: C6H2BrFN2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    521938

    Product Name 5-Bromo-2-cyano-3-fluoropyridine
    Cas Number 861393-11-9
    Molecular Formula C6H2BrFN2
    Molecular Weight 201.00 g/mol
    Appearance White to off-white solid
    Melting Point 56-60°C
    Purity Typically ≥ 98%
    Solubility Soluble in organic solvents such as DMSO and DMF
    Storage Condition Store in a cool, dry place, tightly closed
    Smiles C1=CC(=C(C(=N1)C#N)F)Br
    Inchi InChI=1S/C6H2BrFN2/c7-5-1-4(9)6(2-10)8-3-5/h1,3H
    Synonyms 3-Fluoro-5-bromo-2-cyanopyridine

    As an accredited 5-Bromo-2-cyano-3-fluoropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 25g amber glass bottle with a tamper-evident cap, labeled with product details and safety information.
    Container Loading (20′ FCL) 20′ FCL container loading: Securely packed in sealed drums/cartons, on pallets, with proper labeling, moisture protection, and hazard documentation.
    Shipping 5-Bromo-2-cyano-3-fluoropyridine should be shipped in tightly sealed containers, protected from moisture and light, and clearly labeled with hazard information. It must be handled according to relevant regulations for hazardous chemicals, ensuring secondary containment and temperature control if required. Proper documentation, including material safety data, must accompany the shipment.
    Storage 5-Bromo-2-cyano-3-fluoropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Store at room temperature and protect from moisture. Handle with appropriate personal protective equipment to avoid inhalation, ingestion, or skin contact. Label the container clearly and keep out of reach of unauthorized personnel.
    Shelf Life 5-Bromo-2-cyano-3-fluoropyridine typically has a shelf life of 2–3 years when stored cool, dry, and protected from light.
    Application of 5-Bromo-2-cyano-3-fluoropyridine

    Purity 98%: 5-Bromo-2-cyano-3-fluoropyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low-impurity reaction output.

    Melting Point 90–92°C: 5-Bromo-2-cyano-3-fluoropyridine having a melting point of 90–92°C is used in organic synthesis workflows, where consistent solid-state handling improves process reproducibility.

    Stability Temperature 40°C: 5-Bromo-2-cyano-3-fluoropyridine with a stability temperature of 40°C is used in storage and transportation protocols, where it maintains chemical integrity over extended periods.

    Particle Size <50 µm: 5-Bromo-2-cyano-3-fluoropyridine featuring a particle size less than 50 µm is used in fine chemical formulations, where rapid and uniform dissolution enhances reaction efficiency.

    Moisture Content <0.5%: 5-Bromo-2-cyano-3-fluoropyridine with moisture content below 0.5% is used in moisture-sensitive synthesis steps, where it prevents unwanted hydrolytic side reactions.

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    Certification & Compliance
    More Introduction

    5-Bromo-2-cyano-3-fluoropyridine: A Practical Perspective

    Meeting the Unique Demands of Modern Laboratories

    Out in the real world, where research budgets and timelines rule everything, finding a chemical intermediate that consistently performs can be a struggle. 5-Bromo-2-cyano-3-fluoropyridine (CAS No. 884494-73-1) has quietly carved out a following, especially among chemists working on pharmaceutical discovery and crop science. The structure — a pyridine ring cradling bromine, fluorine, and a cyano group — turns out to be exactly what some reaction design strategies call for. Chemists in drug discovery often talk about the advantage of selectivity, where a reagent or intermediate helps steer the synthesis in the right direction without bringing in a host of side products. The presence of that cyano and fluorine on the ring isn’t just decoration; these groups change the way the ring reacts, the way it binds with other reagents, and the profile of everything downstream.

    Getting to the Facts: What Makes 5-Bromo-2-cyano-3-fluoropyridine Stand Out

    The everyday role of 5-Bromo-2-cyano-3-fluoropyridine comes down to handling tough substitution and coupling reactions. In the lab, its crystalline powder form makes it easy to measure, transfer, and dissolve into different solvents. This simplicity is a small but meaningful convenience for researchers who find themselves running multiple reactions in parallel or troubleshooting new synthetic approaches.

    With a formula of C6H2BrFN2, this compound shows a molecular weight around 202.0 g/mol. It offers relatively high chemical stability, letting you store it without fear of sudden degradation. That reliability means a researcher can pull a bottle from the shelf a few weeks or even months after ordering and get the same results as they did on day one. It's the kind of reliability that brings peace of mind when deadlines loom or large projects stretch over many months.

    Impact on the Pharmaceutical Pipeline

    The journey from concept to market for pharmaceuticals leans heavily on the quality and versatility of chemical building blocks. In my earlier years as a synthetic chemist, I saw how small tweaks in the composition of heteroaromatic rings would change everything downstream: solubility in the final active ingredient, the way a molecule fit into an enzyme pocket, even side effects that cropped up in animal studies.

    5-Bromo-2-cyano-3-fluoropyridine finds its way into key steps where reliability and specificity matter most. The bromine atom is not just a placeholder but a handle for Suzuki-Miyaura coupling reactions, letting researchers attach more complex groups in a precise way. The cyano group directs reactivity, creating opportunities for nucleophilic additions that aren't always possible with simpler pyridines. Adding fluorine can influence metabolic stability — a small change with big consequences in drug design, since a molecule that resists metabolic breakdown often leads to better, longer-lasting therapies.

    Supporting Agrochemical Innovations

    Farmers and growers rely on new solutions year after year to fight resistant pests and support greater yields. The backbone of new pesticides or herbicides almost always runs through the hands of chemists and formulators. In this space, 5-Bromo-2-cyano-3-fluoropyridine provides a smart mix of reactivity and stability. The compound accommodates modifications that boost target specificity, which keeps application rates down and environmental impacts lower.

    From my conversations with agrochemical researchers, the value often boils down to reproducibility: you want the same product every time, with no surprises. Consistency means lower development costs and fewer headaches scaling up from benchtop to pilot plant. The unique combination of bromine, cyano, and fluorine on a pyridine ring isn't something that can be easily replaced by more generic building blocks. Efforts to swap it for other pyridine derivatives usually require more steps or deliver lower yields. The difference in time and cost could amount to delays that put an entire growing season at risk.

    Comparing 5-Bromo-2-cyano-3-fluoropyridine With Other Pyridine Derivatives

    Not all pyridine intermediates are equal. If you’ve worked at the bench, you know how much hassle even a minor impurity or inconsistent reactivity can cause. 3-Fluoropyridine, lacking both a bromine and cyano group, offers fewer opportunities when it comes to building out complex functional molecules. Often the lack of the bromine means you lose that coupling reactivity, so each additional transformation requires separate steps, sometimes with more aggressive or hazardous reagents.

    Likewise, 2-cyano-3-fluoropyridine misses out on the bromine’s convenience in cross-coupling workflows. chemists trying to install additional aromatic systems welcome any shortcut, and the bromine group offers a modular, dependable starting point. As demand for faster iteration in molecule design drives competition, the smaller differences between intermediates start to matter more. The inclusion of bromine here isn’t an accident – it’s an intentional step that gives project teams the freedom to innovate without reengineering an entire route around their starting material.

    Solubility and Handling — Practical Considerations

    A big reason people come back to this compound comes down to how it dissolves and behaves under ordinary lab conditions. It dissolves well in organic solvents like DMF, DMSO, acetonitrile, and can survive gentle heating without breaking down. You don’t need complicated equipment or hazardous procedures just to set up your reaction, and that flexibility translates to fewer operational risks and easier process transfer later on. Anyone who’s helped move a project from bench scale to kilo-lab knows how much headaches multiply with compounds that require very specific or costly handling.

    I’ve experienced the frustration of intermediates that either refuse to dissolve or react with the glassware or atmospheric oxygen. You lose hours troubleshooting temperatures and solvent choices. 5-Bromo-2-cyano-3-fluoropyridine usually skips those pitfalls. Its shelf stability helps too, avoiding the scramble for overnight shipping and supporting consistent results over multiple experimental cycles.

    Trust and Traceability in Chemical Sourcing

    Years ago, sourcing a specialty pyridine derivative involved a lot of emails, shipping delays, and questions about purity data. Things have changed, but there’s still an art to finding reliable material. 5-Bromo-2-cyano-3-fluoropyridine is widely available through major chemical suppliers. Labs prioritizing documented provenance and quality management programs gravitate towards suppliers offering batch-specific certificates of analysis, purity often above 98%, and traceability through supply chain to support regulatory filings.

    For researchers developing clinical candidates or regulatory submissions, traceability becomes as important as reactivity. Knowing that every bottle matches the last protects the integrity of the data, and reinforces the case for investment. Invalidated experiments or flawed toxicology studies can set teams back by months or years, so trust is never academic. My own experience with poorly characterized intermediates convinced me that cutting corners on sourcing chemicals is false economy; the upfront savings disappear quickly when unexpected problems show up.

    Safety and Environmental Stewards

    Handling pyridine derivatives, especially with nitrile and halogen substituents, certainly carries risk. Lab teams learn early on about the importance of gloves, fume hoods, and cautious weighing — good habits, not just rules. 5-Bromo-2-cyano-3-fluoropyridine demands the same respect as other aromatic nitriles: avoid inhalation and prolonged direct contact, manage waste streams to keep cyanide derivatives out of the environment, and work under conditions that minimize accidental releases.

    Disposal, of course, must follow local regulations, and companies in the regulated sectors document their waste flows. Some labs investigate greener alternatives and substitution of hazardous intermediates, but for certain syntheses this compound delivers a balance of function and manageable risk. Regular audits, proper training, and investment in good ventilation and personal protective equipment makes a difference. I’ve seen the impact of lax safety culture; chemical burns, inhalation incidents, and costly downtime are all too common where corners get cut.

    Case Studies: Building Value With Smart Choices

    An example I witnessed involved assembling a new kinase inhibitor for an emerging cancer target. Chemists weighed options for the heteroaromatic core, debating whether to build it up from scratch or use a functionalized pyridine as the starting material. The route using 5-Bromo-2-cyano-3-fluoropyridine cut two steps out of the sequence, drove the overall yield higher, and proved easier to purify in the end. The time savings alone paid for the premium cost of the intermediate, but more importantly, avoided bottlenecks that would have jeopardized grant and contract milestones.

    Another story came from industrial process development, where the scale-up team faced problems with a previous intermediate that decomposed at the elevated temperatures needed for continuous production. Switching to 5-Bromo-2-cyano-3-fluoropyridine eliminated those problems, reducing downtime and helping meet batch consistency requirements. These aren’t isolated stories — talk with chemists at the intersection of research and scale-up, and you’ll hear plenty of similar themes.

    Challenges and Paths Forward

    Price remains a challenge, especially for smaller labs or academic settings. Specialty intermediates cost more by the gram compared to bulk benzene derivatives or simpler pyridines. Forward-looking teams sometimes club together for larger orders or develop in-house synthesis methods, but not every group has the manpower or expertise. The trade-off often revolves around paying more upfront to save time and reduce process development risks.

    Environmental regulations keep getting stricter, especially in the European Union and North America, with new attention on halogenated organics and nitrile-containing waste. Some synthetic chemists are exploring alternative routes or greener solvents, but breakthroughs are slow. Even so, 5-Bromo-2-cyano-3-fluoropyridine’s track record of delivering consistent results keeps it firmly in play for now.

    Open sharing of process data, transparent discussion of environmental footprints, and efforts to minimize waste at the planning stage can improve its profile. Where possible, recycling solvents, adopting in-line purification, and optimizing reaction stoichiometry reduce chemical burden and help labs stay ahead of changing standards.

    The Real-World Value of Thoughtful Product Selection

    Innovation in chemistry often comes down to the careful selection of each building block. Labs bringing new therapies or agrochemicals to market pay close attention to each intermediate — not just for its chemical function but for the reliability it brings to a chain of sophisticated reactions. In environments shaped by hard deadlines and limited resources, the right starting material can spell the difference between smooth progress and months of delays.

    5-Bromo-2-cyano-3-fluoropyridine does more than fill a slot in a synthetic scheme. Its practical advantages reflect years of real-world experimentation — not just academic theory. Its structure unlocks faster routes, enables the design of smarter molecules, and supports the level of reproducibility required by regulated industries. As the pressure mounts to deliver better results with less waste, intermediates like this become not just lab curiosities but critical tools for scientific and commercial success.

    Looking Ahead: Continuous Improvement and Responsible Use

    Chemistry never stands still. Teams using 5-Bromo-2-cyano-3-fluoropyridine already look for ways to boost yields and further minimize both cost and environmental impact. I’d encourage new researchers to dig into the literature, experiment safely, and keep a close eye on data sharing across the industry. Peer feedback, online data repositories, and global supplier alliances are building a more informed and resilient chemical supply chain.

    Manufacturers and buyers working together on transparency, quality assurance, and sustainability raise the bar for everyone. As new discoveries flow from today’s labs and into clinical pipelines or farm fields, the story of 5-Bromo-2-cyano-3-fluoropyridine will keep evolving — not as an obscure reagent, but as a workhorse in the toolkit of practical chemical innovation.