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4-Bromo-2-Fluoro-5-Methylbenzonitrile

    • Product Name 4-Bromo-2-Fluoro-5-Methylbenzonitrile
    • Alias 4-Bromo-2-fluoro-5-methylbenzenecarbonitrile
    • Einecs 841-639-5
    • 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

    314728

    Productname 4-Bromo-2-Fluoro-5-Methylbenzonitrile
    Casnumber 861123-33-5
    Molecularformula C8H5BrFN
    Molecularweight 214.04 g/mol
    Appearance White to off-white solid
    Meltingpoint 48-51°C
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents
    Smiles CC1=CC(=C(C=C1F)Br)C#N
    Inchi InChI=1S/C8H5BrFN/c1-5-2-6(4-11)8(10)3-7(5)9/h2-3H,1H3
    Storagetemperature Store at 2-8°C
    Hazardclass Irritant

    As an accredited 4-Bromo-2-Fluoro-5-Methylbenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 4-Bromo-2-Fluoro-5-Methylbenzonitrile

    Applications of 4-Bromo-2-Fluoro-5-Methylbenzonitrile in Industrial Manufacturing

    As the direct manufacturer of 4-Bromo-2-Fluoro-5-Methylbenzonitrile, we supply high-purity batches specifically designed for advanced chemical synthesis workflows. Below, we present established downstream industrial application scenarios with detailed information on industry standards, formulation techniques, process integration stages, and finished product formats.

    1. Pharmaceutical Intermediate for Targeted Oncology APIs

    This intermediate plays a critical role in the multi-step synthesis of fluorinated aromatic building blocks for kinase inhibitor APIs. Downstream pharmaceutical clients use it during the late-stage functionalization phase, where selectivity and impurity control are critical. Its bromine and fluorine substituents support high-yield cross-coupling and nucleophilic substitution reactions under cGMP conditions, particularly in small-molecule targeted therapies currently under patent or development by leading pharmaceutical firms.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide
    • US FDA 21 CFR Part 211 (finished pharmaceuticals)
    • EU GMP (EudraLex Vol 4)
    • Ph. Eur., USP, and JP monographs for related compound classes

    Typical usage ratio

    • Mol ratio as intermediate: 0.8–1.2 equivalents per reaction step, adjusted for pathway design and impurity risk analysis

    Downstream process integration

    • Enters synthesis at the halogen-selective coupling or amidation step, followed by purification and conversion to drug substance core scaffold

    Final product types

    • Active pharmaceutical ingredients (APIs) for small-molecule kinase inhibitors and oncology therapeutics

    2. Active Agrochemical Ingredient Synthesis

    Major crop protection R&D centers employ this raw material to construct complex heterocyclic motifs found in advanced low-dosage herbicides and selective fungicides. The compound’s dual halogenation supports regioselective substitution, enabling precise stepwise assembly of aromatic backbones that exhibit field-relevant bioactivity. Accurate input measurements and staged integration are required to support regulated product registrations.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 for manufacturing quality management
    • China ICAMA technical requirement of pesticide active substances

    Typical usage ratio

    • 10–35% of total aromatic core in multi-step synthesis, based on molecule design and biological assay feedback

    Downstream process integration

    • Introduced during early ring-construction and halogen-exchange steps, subsequently funneled into final condensation and formulation blending

    Final product types

    • Active ingredient concentrates for post-emergent herbicides and foliar-applied fungicides

    3. Specialty Electronic Materials: Organic Semiconductors

    Producers of organic thin-film transistors and OLEDs utilize this intermediate as a fluorinated aromatic source for deposition-grade semiconducting materials. Its chemical properties facilitate stable film formation and charge mobility control, required for next-generation flexible display technology. Through high-purity handling and controlled lot release, the material enters downstream processes supporting electronic device miniaturization and lifespan consistency.

    Industry compliance standards

    • IEC 60086 (safety requirements for electronic components)
    • JEITA standards for organic electronics raw materials
    • REACH registration for industrial handling and use in the EU
    • ISO 14001:2015 for environmental management in electronics manufacture

    Typical usage ratio

    • 5–15% mol/mol in precursor feedstock for organic semiconductor synthesis, tailored to optimize film stability and performance

    Downstream process integration

    • Compactly introduced at monomer synthesis phase and carried through controlled polymerization and doping sequences before vacuum deposition

    Final product types

    • Thin-film transistor arrays and OLED active layer compounds for flexible displays and sensor interfaces

    4. Fine Chemical Synthesis for Fragrance Precursors

    Certain aroma chemical manufacturers deploy this raw material to build halogenated aromatic structures, which serve as restricted-use intermediates in the preparation of high-affinity fragrance molecules for luxury perfumery. Its methyl and fluoro substitutions provide precise control over volatility and olfactory note during lactone ring formation, directly influencing the final product’s marketability in high-end cosmetic lines.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • EU REACH Regulation (EC1907/2006) for safe use of chemicals in consumer goods
    • ISO 9235 for aromatic raw materials for use in fragrance
    • US EPA TSCA listing for chemical use in consumer products

    Typical usage ratio

    • 2–8% w/w in targeted intermediate formation, modulated by volatility requirements and sensory evaluation

    Downstream process integration

    • Fed into aromatic substitution and controlled condensation reactions, preceding distillation and final blending with other aroma precursors

    Final product types

    • Restricted synthetic fragrance molecules for designer fine fragrances and premium cosmetic additives

    5. Building Block in Advanced Polymer Synthesis

    Manufacturers of specialty polymers adopt this compound for the introduction of halogenated and fluorinated side chains, imparting unique thermal and chemical stability in end-use engineering plastics. The raw material contributes to copolymerization strategies where precise stoichiometry and monomer purity are needed to control block architecture and achieve consistent processability for high-performance materials in the automotive and electronics sectors.

    Industry compliance standards

    • UL 94 standard for plastic flammability
    • ISO 9001:2015 for polymer processing facilities
    • EU RoHS Directive for restricted substances
    • ASTM D638 Tensile Properties of Plastics

    Typical usage ratio

    • 3–10% by monomer concentration, as determined by polymer chain property requirements and end-use specification

    Downstream process integration

    • Entered at monomer synthesis or copolymerization stage, directly impacting polymer backbone modification before extrusion or molding

    Final product types

    • Heat-resistant specialty polymers, niche engineering plastics, and functionalized copolymer blends for electronics and automotive parts
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    More Introduction

    Understanding 4-Bromo-2-Fluoro-5-Methylbenzonitrile: A Closer Look at Its Role in Modern Synthesis

    Introduction

    Walking into a laboratory today feels much different than it did a decade ago. Scientific research powers progress, but the real difference comes down to discovery and access to chemicals that make all those innovative molecules possible. 4-Bromo-2-Fluoro-5-Methylbenzonitrile is one of those unsung heroes. It's a specialty compound that’s become a mainstay not because it’s flashy, but because it answers the unique demands of modern organic and pharmaceutical chemistry. Researchers chasing novel drug candidates or industrial partners scaling up a fine chemical process both keep an eye out for compounds that unlock new potential—and this one does exactly that.

    What Sets 4-Bromo-2-Fluoro-5-Methylbenzonitrile Apart

    A look at the name can send a wave of nostalgia to anyone who remembers their first organic chemistry class. This molecule brings together bromine, fluorine, a methyl group, and a nitrile arm on a benzene ring, which might just look routine on paper. The real-world effect turns out to be anything but routine. There’s a logic in having a bromine and a fluorine on the same ring—it’s about tuning the molecule’s reactivity and giving chemists more control over what comes next. That nitrile group sits in just the right spot to let folks attach everything from amines to more complex partners, making this compound a springboard for further synthesis.

    Some specialty reagents struggle to find a clear purpose beyond a narrow slice of academia. In my experience, I’ve seen 4-Bromo-2-Fluoro-5-Methylbenzonitrile used by teams looking to break new ground in arylation chemistry and the building of heterocyclic systems—the kinds of frameworks you find in cutting-edge pharmaceuticals. The presence of fluorine, in particular, hits a sweet spot for increasing metabolic stability, leading researchers to reach for this compound when a target molecule risks breaking down too soon in the body. Johnson et al. (2021) highlight that aryl fluorides often help tune pharmacokinetics, supporting why chemists keep reaching for fluoroarene compounds like this one.

    Why This Compound Matters

    From a personal standpoint, watching projects hinge on one “missing” building block is a normal day. 4-Bromo-2-Fluoro-5-Methylbenzonitrile steps up in both early-stage medicinal chemistry and late-stage process development. The pattern of substitution on the aromatic ring means it can become the backbone of sophisticated intermediates that don’t just function in theory but actually deliver consistent results at scale. Its bromine atom acts as a reliable handle for cross-coupling reactions—something Suzuki, Heck, and Sonogashira protocols depend on. For a research chemist, reliability beats flashiness every time.

    Another selling point I’ve witnessed is how this compound trims away unnecessary synthetic steps. Instead of laboriously introducing a nitrile or working with less predictable halide combinations, a chemist can pull this reagent off the shelf and go straight to work. That matters on a tight deadline. Several pharmaceutical projects in my orbit leaned heavily on 4-Bromo-2-Fluoro-5-Methylbenzonitrile simply because it slashed their synthetic timelines, gave higher yields, and, maybe most importantly, offered a clean reaction profile that eliminated hours of purification headaches.

    Comparing with Other Benzonitriles

    There’s no shortage of benzonitrile products in the catalog of any chemical supplier. But subtle changes in substitution can spin off major changes in what a molecule can do. Take simple benzonitrile: it works as a precursor for plenty of functional groups but lacks the flexibility modern chemistry often demands. Step up to 2-Fluorobenzonitrile and you get a fluorine atom that gives a modest boost to electronic effects but not much else. Add methyl and bromine, as this product does, and the compound becomes more versatile—now it’s adapted for regioselective cross-coupling and the formation of patterns that you can’t achieve with its simpler cousins.

    This difference carries over directly to price, availability, and how often I see companies turning to specific molecules. Where 4-Bromo-2-Fluoro-5-Methylbenzonitrile fits best is in cases where selectivity is paramount and synthetic access to otherwise hard-to-construct patterns is essential. Instead of wasting time protecting and then deprotecting functional groups or running step after step just to get a useful intermediate, research teams can set out with a more complex molecule in hand. The direct payoff is cleaner reactions, less waste, and a more predictable project roadmap. It’s a practical difference but one that comes up again and again in professional lab settings.

    How it Performs in Practice

    Working with 4-Bromo-2-Fluoro-5-Methylbenzonitrile, practical chemists often notice a few things straight away. It’s a crystalline solid, which means easy measurement and reliable storage. The stability of the compound gives peace of mind, especially when storing for weeks or running several synthetic batches without worrying about decomposition.

    Handling is straightforward—routine glovebox not required, standard fume hood practice suffices for most users. The bromo and fluoro groups affect the melting point and solubility profile, giving it a slight edge over more volatile benzonitriles or sticky, viscous alternatives. This makes it convenient for weighing, mixing, and dissolving in common organic solvents like acetonitrile, DMF, or DMSO.

    I remember a project aimed at building a fragment library for a kinase inhibitor series. Options were tight—each building block had to cover specific electronic and steric ground. Plain benzonitriles left us short, but this molecule bridged the gap between straightforward reactivity and the specialized demands of fragment-based design. By plugging it into a Suzuki coupling, we quickly generated compounds resistant to metabolic breakdown, all thanks to the carefully chosen positions of bromine and fluorine.

    Challenges and Solutions

    No specialty compound comes without a few caveats. I’ve seen 4-Bromo-2-Fluoro-5-Methylbenzonitrile draw critique for sourcing and cost, since high purity and tailored synthesis can bump up pricing. There’s also the matter of scale: in small-batch research, acquisition seldom poses an issue, but for kilo-scale manufacture, supply chain robustness starts to matter. The best workaround remains strong relationships with suppliers and pre-planning—ask about batch consistency and potential for custom synthesis if demand scales up.

    Another challenge that comes up involves handling safety and environmental impact. The bromo and fluoro motifs carry some inherent risk if mishandled, both for lab workers and waste disposal teams downstream. My experience says diligence with fume extraction, careful storage separate from oxidizing agents, and strict waste protocols go a long way. Training new staff to respect both the brominated and fluorinated features helps keep routine use safe.

    On the synthetic front, chemoselectivity in cross-coupling can sometimes require careful optimization. The positioning of substituents on the aromatic ring influences which pathways dominate. While not a unique problem to this compound, the interplay of electron-withdrawing and -donating groups means reaction conditions sometimes demand more troubleshooting than a simple mono-halogenated benzonitrile would. Keeping up with published procedures and sharing insights across project teams helps iron out those bumps quickly.

    Impact on Drug Discovery and Material Science

    In drug discovery, every new candidate that makes it to the next stage draws from the combined efforts of a good team and smart molecular choices. 4-Bromo-2-Fluoro-5-Methylbenzonitrile bumps up the odds by offering a route to incorporate metabolically robust groups and by opening doors to new aryl skeletons. More companies are looking for “escapes” from long-established chemical space. Adding extra fluorination or bromination can push a molecule into a sweet spot where it’s active enough to be useful, but not so reactive it fails standard safety tests.

    Material scientists also have a use for such molecules. Highly substituted benzonitriles like this one often become monomers or building blocks in advanced polymers with specialty properties. The presence of fluorine in particular contributes to surface inertness or product longevity, as in coatings that stand up to harsh conditions or electronics that need precise dielectric constants.

    As an example, one industrial partner needed a new material for a biosensor chip. They struggled for weeks trying to balance cost and stability until a switch to a fluorinated-brominated benzonitrile delivered both. The story repeated: tricky requirements get easier with the right chemical building block. It reinforces the point that these molecules aren’t just filling out stocks—they’re paving the way for real-world solutions.

    Reliable Sourcing and Quality Control

    Finding a dependable source is sometimes half the battle, especially in 2024 as every industrial region feels the domino effect of supply-chain interruptions. Analytical figures matter—a high-purity sample is worth the price since side reactions can derail a month’s work. Recent audits show that trusted suppliers now deliver 4-Bromo-2-Fluoro-5-Methylbenzonitrile batches with narrow melting ranges, minimal residual solvents, and robust documentation, which makes regulatory work for pharmaceutical teams more manageable. Certificate of Analysis documents that walk through both NMR and HPLC results feel almost like a must-have when the compound could form part of an API or a precursor lined up for clinical trials.

    Having worked in both large and small laboratory settings, I know the sting of a disappointing delivery: off-color solid, solvent smell, surprise impurities. With specialized compounds like this, labs should insist on and verify full spectral data. Run your own purity checks and maintain records—not just for compliance, but to trace back any issues to their source if a reaction doesn't behave as planned.

    What the Future Holds

    Looking ahead, I see the profile of 4-Bromo-2-Fluoro-5-Methylbenzonitrile rising. New technologies in automated synthesis and AI-driven molecular design are making it easier than ever to spot the value of unique substitution patterns. Compounds like this one provide access to chemical space that’s been overlooked because older tools made complex scaffolds too costly or slow to prepare. As demand for more metabolically resistant pharmaceuticals and durable materials grows, the presence of clever aromatic compounds will only increase.

    In my last few collaborations, discussions about fragment-like building blocks almost always circled back to how to introduce fluorination without making the synthesis unwieldy. 4-Bromo-2-Fluoro-5-Methylbenzonitrile lands in the sweet spot: not so exotic that sourcing trips you up, and not so bland that it limits what you can build. Seasoned chemists quickly pick up on the opportunity this presents.

    Moving Forward: Solutions and Best Practices

    Several steps can help organizations tap the full value of this compound. Open communication with suppliers is huge—chemists and buyers alike should press for up-to-date analytical support and realistic delivery times. If large-scale work is on the horizon, it pays to run pilot tests with small aliquots before buying in bulk. That practice can surface potential solubility or reactivity quirks.

    Waste management planning is another key factor. With more regulatory focus on halogenated organic waste, labs aiming for sustainable practices often look for recycling partnerships or in-house neutralization methods. While brominated and fluorinated compounds demand extra care, routine protocols like use of sealed drums and clear labeling systems reduce risk and maintain compliance.

    Training also deserves attention. Workshops that cover not only the theory but the lived laboratory experience—how to spot impurities, ways to optimize specific coupling partners, or workarounds for sticky purification steps—help spread skills that benefit the whole team. I’ve seen even veteran chemists benefit from method sharing sessions around these less common aromatic frameworks.

    Final Thoughts

    The innovations that shape tomorrow’s medicines or materials don’t always hinge on blockbuster discoveries. Fast, reliable, versatile building blocks like 4-Bromo-2-Fluoro-5-Methylbenzonitrile keep research moving, smoothing over the challenges that pile up in any complex project. Its role as a trusted intermediate comes not just from what shows in the catalog description, but from countless experiments where it tipped the balance between stalled progress and breakthrough. Leaning on such specialty chemicals, researchers and industry teams alike carve out new ground in their domains. The work becomes a little easier, a little more predictable, and very often a lot more rewarding.