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5-Bromo-3-Fluoro-Pyridine-2-Carbonitrile

    • Product Name 5-Bromo-3-Fluoro-Pyridine-2-Carbonitrile
    • Alias 5-Bromo-3-fluoro-2-cyanopyridine
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    Specifications

    HS Code

    541951

    Chemical Name 5-Bromo-3-Fluoro-Pyridine-2-Carbonitrile
    Molecular Formula C6H2BrFN2
    Molecular Weight 201.00 g/mol
    Cas Number 144584-62-9
    Appearance White to off-white solid
    Melting Point 67-70°C
    Purity Typically >98%
    Solubility Soluble in organic solvents such as DMSO, DMF, and chloroform

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

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    Application of 5-Bromo-3-Fluoro-Pyridine-2-Carbonitrile

    Applications of 5-Bromo-3-Fluoro-Pyridine-2-Carbonitrile in Industrial Manufacturing

    Our factory-synthesized 5-Bromo-3-Fluoro-Pyridine-2-Carbonitrile plays an integral role in advanced chemical manufacturing, where performance, safety, and regulatory compliance guide each downstream application. The following industrial application scenarios detail the specific end-use environments, compliance benchmarks, practical incorporation methods, and final product forms adopted by professionals utilizing this specialty intermediate.

    1. Pharmaceutical Intermediate for Antiviral Drug Synthesis

    This raw material functions as a precursor in the custom synthesis of pharmaceutical APIs, particularly within the synthesis of heterocyclic building blocks essential for antiviral compounds. The structure introduces both bromine and fluorine moieties, aiding in biological activity optimization necessary for drug candidate progression. Regulatory expectations demand traceability within multistep synthesis processes, and batch-specific integration occurs at defined stages to control impurity profiles and achieve accurate final API characteristics.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Manufacturing
    • European Pharmacopoeia (Ph. Eur.) synthesis precursor criteria
    • US FDA 21 CFR Part 211 – cGMP for finished pharmaceuticals
    • REACH Annex IV/V compliance for intermediates

    Typical usage ratio

    • 0.5–2.2 molar equivalents per reaction batch; exact levels are adjusted depending on stoichiometric pathway and required functionalization of the core pyridine ring.

    Downstream process integration

    • Employed in the early to mid-stages of multi-step heterocycle construction via nucleophilic aromatic substitution or Suzuki coupling protocols.
    • Introduced after initial framework assembly, before final amination or selective protection/deprotection steps.

    Final product types

    • API intermediates for small-molecule antiviral drugs
    • Key intermediates for kinase inhibitor compounds
    • Building blocks for custom drug candidate libraries

    2. Agrochemical Intermediate in Active Ingredient Synthesis

    Major agrochemical enterprises rely on this raw material during the assembly of pyridine-based herbicides and insecticides, due to its dual halogenated profile that improves target molecule reactivity, enhances field stability, and modulates environmental fate. Rigorous batch documentation and trace impurity control are implemented to assure crop safety and product stewardship throughout the supply chain. Process optimization locally controls the introduction of the fluorobromo pyridine moiety to fine-tune active ingredient profiles.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • OECD GLP for environmental chemistry and residue analysis
    • ISO 9001:2015 for quality management systems in agrochemical plants
    • EU Regulation (EC) No 1107/2009 – Plant Protection Products

    Typical usage ratio

    • 0.8–1.5 equivalents in coupling reactions; varies by target molecule structure and desired halogenation density on final agrochemical active.

    Downstream process integration

    • Incorporated in the nucleophilic substitution and C–C coupling stage during late phase synthesis of active agrochemical ingredients.
    • Post-reaction work-up targets separation from overbrominated or underfluorinated side products for regulatory residue minimalization.

    Final product types

    • Precursor intermediates for selective herbicides targeting grass weeds
    • Halogenated insecticide scaffolds for custom pesticide solutions
    • Pyridyl fungicide precursors optimized for broad-spectrum crop protection

    3. Advanced Material Intermediate for Liquid Crystal Display (LCD) Chemicals

    Producers of specialty intermediates for LCD materials incorporate this compound as a halogen-selective input for designing highly responsive fluorinated pyridine cores, influencing mesophase behavior and dielectric properties in liquid crystal formulations. Careful control of the addition within fluorination or cross-coupling units at industrial plants ensures performance consistency for downstream display panel manufacturing. Documentation is maintained for high-purity standards and proprietary process traceability, supporting international OEM qualification requirements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for electronics chemicals supply
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • IECQ QC 080000 – Hazardous Substance Process Management
    • JIS C 61000 – Japanese LCD chemicals and electronics ingredient standards

    Typical usage ratio

    • 0.3–0.9 equivalents per batch; calculated to achieve fine-tuned halogen content for dielectric performance and thermal stability in the final blend.

    Downstream process integration

    • Utilized at the initial stage of liquid crystal core structure building, typically during Suzuki–Miyaura or Stille coupling reactions to obtain required fluorinated pyridine orientations.
    • Integrated prior to polymerization or crosslinking step in advanced liquid crystal precursor formulations.

    Final product types

    • Mono-halogenated liquid crystal intermediates for TFT-LCD production
    • Fluorinated aromatic building blocks for high-purity display chemicals
    • Dielectric active materials used in flexible OLED and advanced screen substrates

    4. Fine Chemical Intermediate for Specialty Dye Manufacturing

    Manufacturers in the specialty dyes sector utilize this compound for the targeted synthesis of pyridine-substituted chromophores and pigments. Its halogen profile empowers the development of color-stable and chemically resistant dye molecules for demanding application environments such as photographic films, industrial inks, or lightfast coatings. Specialized integration protocols ensure traceable handling, efficient coupling with color-intensifying agents, and precise endpoint characterization—all of which align with international dye production regulations.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substance in dyes
    • EU REACH compliance for industrial aromatic intermediates
    • ISO 1833 for textile dye quality analysis
    • EN 71-3:2019 for pigments used in toys and consumer products

    Typical usage ratio

    • 1.0–1.3 molar equivalents; levels are fine-tuned to balance halogen loading with chromophore stability and shade consistency as specified in customer dye recipes.

    Downstream process integration

    • Introduced in the condensation or azo-coupling stage into pyridine-containing dye structures.
    • Precisely metered into reaction vessels for stepwise halogen introduction, ahead of final diazotization or alkylation.

    Final product types

    • Lightfast azo and anthraquinone dyes used in industrial printing
    • Pyridine-based specialty pigments for automotive coatings
    • Photographic sensitizer dyes requiring elevated chemical resistance
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    More Introduction

    Introducing 5-Bromo-3-Fluoro-Pyridine-2-Carbonitrile: Value and Versatility in Modern Chemistry

    Understanding the Compound

    5-Bromo-3-fluoro-pyridine-2-carbonitrile stands out in the laboratory for its practical applications and solid reputation among synthetic chemists. This compound features a fused aromatic ring structure, with a bromine atom at the five position, a fluorine at the three, and a cyano group at the two position—an arrangement that makes it more than just another specialty reagent. Anyone who has stood in front of a fume hood eyeballing a stubborn coupling reaction knows the headaches of unpredictable reactivity. The structural reliability and predictable behavior of this molecule has saved many a research timeline. Its chemical formula, C6H2BrFN2, reflects the unique combination of halogen and cyano substituents.

    Choosing the Right Form: Model and Specifications

    A key factor in lab work is consistency. Chemists have learned that not all fluorinated pyridines behave the same way. 5-Bromo-3-fluoro-pyridine-2-carbonitrile comes in an off-white crystalline powder, stable under standard storage conditions, and doesn’t tend to clump or cake, which many who’ve handled less stable reagents will appreciate. Typical impurities remain low since synthetic routes yield this molecule in high purity—most high-quality batches reach above 98%. Melting points hover around 108-110°C, which can be checked easily in-house to confirm identity and purity. Shelf-life does not usually pose issues; I’ve kept well-sealed samples for well over a year without any compositional shift on NMR or LCMS.

    Material safety deserves a mention, too. Brominated and fluorinated aromatics can sometimes irritate the skin or respiratory tract, so anyone handling this product should respect basic protective procedures: gloves, goggles, and a well-functioning extraction system keep working conditions safe and comfortable.

    How Chemists Get the Most Out of Its Structure

    The uses for this compound go well beyond single-step reactions. In my experience in small-molecule synthesis labs, it often plays a role in the construction of complex drug candidates. The electron-withdrawing properties of the cyano, fluoro, and bromo groups open up possibilities that simple pyridines or mono-substituted analogs just don’t offer. Medicinal chemists often turn to this compound during lead optimization, exploring new analogs for anti-viral or anti-cancer properties. A single halogen swap can drastically change metabolic stability or target affinity. Adding the cyano group at the ortho position, with a bromo and a fluoro further modifying the ring, results in a behavior profile vastly different from a plain pyridine. It’s not uncommon to see this molecule at the root of scaffolds for kinase inhibitors, anti-inflammatory molecules, or agrochemical candidates.

    In my own projects, swapping out the bromo for another group with a Suzuki coupling is a routine approach. The clean reactivity helps avoid byproducts. The cyano group, thanks to its stability, enables further nucleophilic substitutions, and selective metalations don’t turn the product into a mess, unlike many less-forgiving substituted pyridines.

    From Analogues to Stand-Alone Utility

    The story of pyridine derivatives is long, with each new substituent unlocking distinct patterns. 5-bromo-3-fluoro-pyridine-2-carbonitrile consistently delivers results that less-substituted or differently-substituted pyridines just can’t match. For example, compare this compound to a 2-cyanopyridine with no halogens—without the bromo, palladium-catalyzed cross-coupling efforts often stall or lead to low yields. Without the fluorine, regioselective functionalization loses reliability.

    In classes and on the lab bench, the differences become clear. Fluorine atoms invite specific hydrogen bond interactions, raising the possibility of tighter ligand-protein binding in biological systems. Bromine, with its bulk, can direct reactivity, allowing for precise additions not feasible otherwise. When both are present and paired with a cyano, this trifecta accelerates method development in both academic and industrial contexts.

    Impact on Method Development and Process Optimization

    Process chemists prize molecules that maintain their integrity under a range of conditions. I’ve seen batches of this compound hold up nicely to mild acid or base, which saves both time and money in scale-up. Details matter—if an intermediate decomposes after a day on the bench, it throws off schedules and budgets. From a process standpoint, the combination of manageable melting point, high purity, and predictable reactivity simplifies purification protocols down the line.

    In pharmaceutical manufacturing, route scouting becomes more efficient when the key building block behaves reliably batch after batch. It can take months to optimize a synthetic route, and starting materials that change the rules make things harder. Whether using microwave promotion or classical reflux, 5-bromo-3-fluoro-pyridine-2-carbonitrile consistently matches expectations.

    Comparisons to Similar Pyridine Building Blocks

    Many chemists try to substitute other pyridines to cut costs, but they often return to this molecule for a reason. Mono-halogenated pyridines fall short during library synthesis, with either sluggish reactivity or troublesome side-products. Even dual halogenated analogs, unless carefully positioned, can complicate regioselective transformations. Multi-halogenated versions without the cyano group sometimes lead to instability or fail in steps that demand electron-withdrawing support.

    Compared to compounds like 3-bromo-2-cyano-pyridine, the extra fluorine atom at the three position in 5-bromo-3-fluoro-pyridine-2-carbonitrile introduces new selectivity options, especially in SNAr chemistry or palladium-catalyzed couplings. As someone who has juggled a dozen different building block candidates trying to generate lead-like small molecules, the value of reliability grows the nearer a project moves toward scale-up. In agrochemical synthesis, these differences equate directly to cost and regulatory hurdles, since cleaner reactions mean less work at the analysis and compliance stage.

    Sustainability and Environmental Considerations

    Every year sustainability takes up more space in purchasing and research discussions. Many modern labs evaluate the full life-cycle of a chemical, from manufacturing principles to waste management. 5-bromo-3-fluoro-pyridine-2-carbonitrile lends itself fairly well to these conversations, especially since the high-yielding synthetic methods for this compound limit side-products and waste streams. Trends in green chemistry point toward reagents that balance reactivity with environmental responsibility; compounds that generate minimal byproducts step into the spotlight.

    Chemists outside the bench—think procurement managers, EHS officers—look at metrics like atom economy and ease of downstream waste neutralization. With fewer purification demands and less reactive waste, the compound nudges projects toward the benchmarks demanded by regulatory agencies. Having witnessed the headaches that come with unwieldy byproduct profiles, I can say that practitioners often rally behind reagents like 5-bromo-3-fluoro-pyridine-2-carbonitrile because safer and cleaner syntheses also make economic sense.

    The Impact on Research Timelines

    Research never sticks to a schedule. Unexpected delays crop up, whether from unreliable shipments or tricky intermediates giving inconsistent yields. Researchers remember the compounds that work every time, under standard conditions, with as few surprises as possible. 5-bromo-3-fluoro-pyridine-2-carbonitrile boasts a track record in academic and private-sector labs. Scientists developing libraries of analogs need to secure reproducible outcomes, not repeat purification cycles on unpredictable batches.

    With cleaner NMR spectra and LCMS profiles, analytical teams also spend less time tracking down mystery peaks or degradation products. I’ve watched teams breathe easier knowing their intermediate will hold together long enough to finish a standard reaction, or sit safely for a few days if an experiment needs to be pushed.

    Opportunities for Further Development

    Discovery chemistry keeps pushing for more effective and focused building blocks. Adding functionality to pyridine rings continues to fuel new patents every year. Industry trends show that companies invest more in multi-functionalized scaffolds to expand the window of chemical diversity. 5-bromo-3-fluoro-pyridine-2-carbonitrile fits right into that landscape. Incorporating select halogens and a cyano group offers distinct branching points, inviting selective modifications at each step. As a result, the molecule’s utility extends beyond simple library synthesis to highly targeted, structure-activity relationship studies.

    Scientists working on new pharmaceuticals look for early indicators that a scaffold will prove "druggable." Fluorine atoms can influence metabolic pathways; bromine eases downstream couplings. The cyano group’s ability to serve as a masked amine or carboxylic acid segment opens various late-stage derivatizations. Even outside pharma, the same structural features unlock routes in advanced materials science, whether stabilizing dyes or developing new catalysts.

    Building Confidence Through Evidence

    Trust plays a powerful role in chemical sourcing. Not every batch from every producer meets expectations. Labs that have built up experience with 5-bromo-3-fluoro-pyridine-2-carbonitrile regard it as dependable precisely because its purity and integrity remain high across suppliers that publish analytical data. Checking a COA and examining the spectroscopic signatures before signing off on a batch become routine safeguards.

    Scientific literature backs up the growing embrace of this building block. In peer-reviewed journals, dozens of synthetic pathways cite this compound as a core intermediate, with side-by-side data points supporting its clean reactivity and reproducibility. Even patent literature increasingly lists this product, confirming both its commercial and intellectual property value.

    What Could Be Improved?

    No product is perfect. Halogenated organics still pose some handling and disposal issues, and like many specialty reagents, costs can spike due to raw material scarcity or transportation. Labs searching for alternatives to hazardous reagents hope for ever-safer synthetic routes, perhaps using less hazardous brominating or fluorinating agents. There’s also space for innovation in packaging—airtight, resealable containers cut down on waste and repeated purchases, and some companies have begun experimenting with more eco-friendly materials without compromising the shelf-life.

    From an operations perspective, bulk-scale availability sometimes fluctuates. Establishing stable global supply lines helps keep research on track. Collaborative procurement—where institutions or enterprise groups combine their orders—puts pressure on manufacturers to streamline processes and secure better pricing for everyone involved.

    Potential Solutions to Industry Challenges

    Feedback from end users often drives change. Direct communication between synthetic chemists and manufacturers encourages the development of updates to existing production methodologies. Greener synthetic routes, including catalytic halogenation under milder conditions, earn interest from companies looking to reduce their chemical footprint and liability.

    Universities and industrial R&D departments have begun exploring continuous flow techniques for preparing this compound, a move that promises enhanced safety and greater batch consistency. Over time, advances in process chemistry should expand access and reduce costs, making reliable building blocks like 5-bromo-3-fluoro-pyridine-2-carbonitrile available to a wider audience.

    Scaled-up recycling efforts for spent brominated and fluorinated organics, along with educational initiatives to ensure best practices in handling and disposal, help reduce the overall footprint. Lab managers can encourage these steps by keeping up-to-date with the latest best-practice guidelines and partnering with suppliers that commit to transparency on sourcing and environmental responsibility.

    Facing the Future With Confidence

    Chemical research moves fast. Every month brings new reagents, new strategies, and new challenges. Familiarity and proven performance matter more than ever. Having worked with an array of pyridine derivatives, and specifically 5-bromo-3-fluoro-pyridine-2-carbonitrile, the compound’s role in modern chemistry feels secure. It delivers well-defined reactivity, solid handling characteristics, and versatility that analysts and synthetic chemists both appreciate.

    Growing pressure on cost, safety, and environmental impact will keep pushing researchers and suppliers to refine these molecules. Partnerships between academia, industry, and regulatory agencies stand to bring out upgrades and efficiencies that help streamline the journey from idea to prototype to market.

    Ultimately, 5-bromo-3-fluoro-pyridine-2-carbonitrile earns its place in the toolkit for its ability to bridge the gap between the practical and the innovative, serving scientists chasing everything from life-saving medicines to advances in fine chemical production. With a sharp focus on reliability and adaptability, the compound’s relevance continues as labs chart the next successes in chemical discovery.