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2-Fluoro-4-Cyanobenzyl Bromide

    • Product Name 2-Fluoro-4-Cyanobenzyl Bromide
    • Alias 2-Fluoro-4-(bromomethyl)benzonitrile
    • Einecs 837-233-6
    • 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
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    792719

    Product Name 2-Fluoro-4-Cyanobenzyl Bromide
    Cas Number 1027519-64-3
    Molecular Formula C8H5BrFN
    Molecular Weight 214.04
    Appearance White to off-white solid
    Purity Typically ≥97%
    Melting Point 47-51°C
    Smiles C1=CC(=C(C=C1Br)F)C#N
    Inchi InChI=1S/C8H5BrFN/c9-5-3-2-6(10)8(1-5)4-11/h2-3H,1H2
    Solubility Soluble in organic solvents (e.g., DMSO, dichloromethane)
    Synonyms 2-Fluoro-4-cyanobenzyl bromide; 4-Bromo(methyl)-2-fluorobenzonitrile

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

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 2-Fluoro-4-Cyanobenzyl Bromide, securely sealed and labeled with hazard and handling information.
    Shipping 2-Fluoro-4-cyanobenzyl bromide is shipped in tightly sealed containers, protected from moisture and light, and cushioned to prevent breakage. Transportation complies with hazardous material regulations, requiring appropriate labeling and documentation. The substance should be kept cool, dry, and away from incompatible materials, with all handling performed by trained personnel using suitable protective equipment.
    Storage 2-Fluoro-4-cyanobenzyl bromide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat, ignition sources, and incompatible materials such as strong oxidizers and bases. Protect from light and store at room temperature or as recommended on the safety data sheet (often 2–8°C). Use proper chemical storage protocols and label clearly.
    Application of 2-Fluoro-4-Cyanobenzyl Bromide

    Applications of 2-Fluoro-4-Cyanobenzyl Bromide in Industrial Manufacturing

    As a direct producer with advanced fluorination and fine organic synthesis capabilities, we supply 2-Fluoro-4-Cyanobenzyl Bromide to key sectors where its unique structure and reactivity are critical for advanced chemical intermediates. Below, we detail core industrial scenarios and how this material fits within each manufacturing environment.

    1. Agrochemical Intermediate Synthesis

    Leading agrochemical companies use this compound for targeted modifications during synthesis of novel pyridine- and pyrimidine-based crop protection agents. Chemists leverage its fluoro and cyanide moieties to achieve specific selectivity in nucleophilic aromatic substitution, forming key intermediates for proprietary active substances. The high purity and controlled particle size from our facility support accurate dosing at scale-up, while the benzyl bromide group allows efficient downstream coupling with heterocyclic scaffolds under controlled temperature and pressure.

    Industry compliance standards

    • REACH (EC) No 1907/2006
    • ISO 9001:2015 Quality Management System
    • Agrochemical-specific regulatory filings (EU PPP, US EPA, GB Standards)
    • Chinese Pesticide Registration Standards (ICAMA)

    Typical usage ratio

    • 0.8–2.5% of total batch weight, dependent on the target protection agent and process scale; formulation chemists optimize within this range based on reactivity studies and desired intermediate yield.

    Downstream process integration

    • Added during Stage II or III of stepwise multi-component synthesis, post-coupling of aromatic core, in jacketed glass-lined reactors under nitrogen.
    • Neutralization and phase separation downstream handled with in-line extraction or aqueous workup.

    Final product types

    • Herbicide intermediates (e.g., fluorinated benzyl derivatives for pyridine carboxylates)
    • Insecticidal building blocks (for novel neonicotinoid structures)
    • Fungicide synthons

    2. Pharmaceutical Intermediate Manufacturing

    Pharmaceutical fine chemical producers rely on this compound for synthesis of fluorinated API precursors, where electron-withdrawing effects and enhanced metabolic stability are essential. It serves in Grignard or Suzuki couplings en route to active benzyl-substituted heterocycles, supporting next-generation kinase inhibitor and CNS application pipelines. Batch consistency ensures reproducible medicinal chemistry R&D, and our analytical documentation supports full traceability in regulated environments.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA cGMPs)
    • European Pharmacopoeia (Ph. Eur.) requirements for residual solvents and impurities
    • Pharmaceutical Excipient Standards (USP/NF, JP, ChP as relevant for registration)

    Typical usage ratio

    • 1.0–3.2% of overall batch composition, adjusted by process chemist depending upon route and scale of target API precursor—higher end for 2-step arylation, lower end when entering as secondary nucleophile.

    Downstream process integration

    • Introduced as acylation or alkylation agent after protection-group chemistry; employed in sealed reactors with real-time GC monitoring for endpoint determination.
    • Purification via silica or reverse-phase column chromatography as needed for in-process quality control.

    Final product types

    • Fluorinated benzylated bioactive intermediates
    • CNS drug precursors (e.g., for antipsychotic or antidepressant targets)
    • Kinin and kinase inhibitor scaffolds

    3. Specialty Material Monomer Production

    Producers of high-performance polymers and specialty electrolytes employ this raw material for custom monomer synthesis, where the fluorinated ring structure introduces chemical resistance and functional group compatibility. Materials engineers select it for chain-stop agents or as a precursor in step-growth or living polymerization, achieving target dielectric, hydrophobic or thermal characteristics sought for electronics or membrane materials.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management
    • RoHS (Restriction of Hazardous Substances) compliance for relevant electronic applications
    • GHS labeling & handling under OSHA/CLP
    • Chemical Substances Control Law (Japan, for advanced materials)

    Typical usage ratio

    • 0.5–1.5% by mass in step-growth or living anionic polymerization feeds; formulation chemists may adjust within this window based on desired functionalization index and copolymer tacticity.

    Downstream process integration

    • Dosed into monomer synthesis reactors prior to initiation, followed by precision metering in polymerization lines; post-polymerization workup via solvent precipitation and controlled vacuum drying.

    Final product types

    • Fluorinated specialty monomers (for advanced resins)
    • Electrolytic polymer precursors (for battery and capacitor applications)
    • Functionalized polymer intermediates for ion-exchange membranes

    4. Liquid Crystal Compound Manufacturing

    Producers of advanced display and sensor components use this chemical for synthesizing fluorinated aromatic liquid crystal building blocks. Its molecular structure enables precise tuning of dipole moment and anisotropy, supporting high-contrast, narrow bandgap formulations for flat panel displays and advanced optical filters. The controlled synthesis environment in our facilities assures purity and low trace contamination, critical for stable mesophase properties.

    Industry compliance standards

    • IEC 62321-7-1:2015 (Halogen determination for display industry)
    • JIS K 7120 (Testing Methods for Liquid Crystals, Japan)
    • RoHS and WEEE directives (for electronics, EU)
    • ISO 9001:2015 for electronic material manufacturing

    Typical usage ratio

    • Ranges from 0.7–1.8% of total formulation mass, optimized for the desired birefringence and dielectric constant in the final mesogen blend.

    Downstream process integration

    • Undergoes haloalkylation in a two-step process, followed by coupling in automated batch reactors at reduced pressure. Final liquid crystal mixture prepared via solvent blending and molecular sieving.

    Final product types

    • Mesogenic intermediates for LCD and OLED displays
    • Optically active films for sensor arrays
    • Fluorinated nematic or smectic liquid crystals
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    Certification & Compliance
    More Introduction

    Introducing 2-Fluoro-4-Cyanobenzyl Bromide: A Chemist’s Perspective

    Shaping Research with Advanced Building Blocks

    Back at our site, the quest for reliable chemical building blocks never really stops. Among the shelves lined with raw intermediates, one compound stands out not just for its versatility but for the way it shapes a broader range of research and manufacturing: 2-Fluoro-4-Cyanobenzyl Bromide. Our journey with this compound reflects the demands and aspirations of both seasoned researchers and production teams requiring unique molecular functionality.

    What Sets 2-Fluoro-4-Cyanobenzyl Bromide Apart

    Experience in the lab drives home the value of a compound that brings more than one functional group to a reaction. This hybrid benzyl bromide equips chemists with both a cyano and a fluorine substituent, opening diverse possibilities for synthesis. From our own benchwork, the unique makeup has proven effective in custom ligand design, fluorinated pharmaceutical intermediates, and the modification of aromatic ring systems where electron-withdrawing effects matter.

    Specifications and Purity: Not Just Numbers

    Years formulating and scaling up teach that numbers on a spec sheet turn meaningful only when they show up in the final results. Our batches exceed 98% purity, and we routinely secure sharp melting points and clear NMR spectra. Operating at this high standard makes the material a trusted choice, not only in academia but in industrial routes where downline purity saves time and costs. Risks from side-products and residual contaminants drop considerably. Process engineers often comment on the stability in shipment and storage, a trait that owes as much to stringent packing as to the rigidity of the molecule itself.

    Why This Benzyl Bromide Gets the Nod

    Traditional benzyl bromides lack substituents tailored for both electronic influence and synthetic flexibility. Many users come from a background of simple alkyl bromides or halo aromatics and recall added synthetic steps needed just to introduce cyano or fluoro groups. Our 2-Fluoro-4-Cyanobenzyl Bromide brings those groups pre-installed, skipping excessive derivatization and streamlining timelines for novel compound development. Compared side-by-side, the yield and selectivity advantages grow evident over single-functionalized commercial alternatives.

    Downstream Performance in Pharmaceuticals

    In the pharmaceutical sector, the cyano handle’s reactivity under mild nucleophilic addition and condensation conditions has supported the discovery of new heterocycles and kinase inhibitors. Chemists working on fluorine-rich scaffolds value how the para-fluoro group introduces metabolic stability without sacrificing reaction rates during subsequent transformations. Over countless reactions, our process avoids excessive by-products such as dibromo derivatives or defluorinated species, which demand downstream purification resources.

    Special Considerations in Agrochemical Synthesis

    For plant protection compounds or emerging agrochemical structures, the priorities run beyond yield. Incorporating fluorine can mean enhanced pest resistance or altered bioavailability profiles. From practical trials and customer feedback, this building block has improved the selectivity and durability of final products. The cyano group grants room for further functionalizations: amidoximes, heterocycles, and tailored ureas. The bromide’s reactivity allows for controlled stepwise reactions, minimizing waste and cutting overall batch costs.

    Comparison Against Structural Analogs

    In screening alternatives like 4-Fluorobenzyl Bromide or 2-Cyanobenzyl Bromide, the dual substitution pattern delivers increased synthetic leverage. Single-function analogs require additional reactions, greater time investment, and more raw materials. Observing runs on a pilot scale clarifies how this product consolidates and simplifies workflows for custom aromatic derivatives. The reactivity-modifying influence of both fluorine and cyano often produces cleaner conversions with less polymerization during nucleophilic substitution steps. These real-world gains have outweighed the slight premium attached to this multi-functional building block.

    Handling and Storage in Real-World Applications

    Bringing years of experience in both hazards and shelf life, we focus on inert atmosphere filling and tight sealing, particularly in locations prone to moisture swings. Benzyl bromides with multiple substituents can sometimes release HBr or undergo slow hydrolysis. With the fluoro and cyano substituents, increased crystallinity and decreased volatility have resulted in more stable shipments. Labs using our material frequently report extended usability, provided storage stays cool and dry. Our own stability trials, even under fluctuating warehouse conditions, revealed no significant degradation over six months, supporting both bulk purchase and steady supply for continuous operations.

    Safe Use and Environmental Impact

    Every shipment comes with close attention to proper use, and every release meets not only purity expectations but also compliance with hazardous substance directives. Drawing from prior incidents, identifying and mitigating bromide activation hazards matters just as much as synthetic utility. Compared with some halogenated benzyl bromides, our product’s relatively low volatility and high crystallinity mean that workplace exposure risks remain controlled with standard bench protections. In waste management, the cyano and fluoro groups do challenge simple degradation protocols, so all downstream partners receive support on compliant disposal methods.

    A Chemist’s Take on Trends in Intermediate Sourcing

    Traditional supply models relied on commodity intermediates and extensive in-house derivatization. In recent years, molecular complexity demands stronger expertise around functionalized aromatics. Customers increasingly want ready-to-incorporate intermediates, saving both man-hours and plant resources. We noticed that adoption rates for our 2-Fluoro-4-Cyanobenzyl Bromide rose quickest among small synthesis labs, custom API shops, and contract research organizations (CROs), where staff juggle tight project schedules and high expectations for innovation. The compound’s design aligns with these pressures. By providing more than a simple reactive handle, it widens the synthetic toolbox and fits the rapid cycle of early-stage molecule development.

    Supporting Informed Choices Through Data and Dialogue

    Our emphasis lies not just in making a product but fostering a knowledge exchange with end-users. Reports from medicinal chemistry teams often cite increased output per FTE when the right building block collapses several steps into one. On expanding manufacturing campaigns, having a robust QC protocol and dependable product flow allowed several CROs to shift away from stockpiling, freeing capacity for more advanced syntheses. Supplier support in troubleshooting batch problems or sharing historical analytical data makes the difference, especially with challenging heteroaromatic couplings.

    Meeting Market Demands with Consistent Quality

    Consistency defines trust in the specialty chemicals arena. Routine analysis—HPLC, GC-MS, NMR—goes beyond marketing. Our labs have tackled batch-to-batch impurities in the past and adapted by refining purification loops and switching to higher-grade bromination reagents. This attention to detail pays off in fewer surprises during scale-up. As more manufacturers standardize their processes around highly functionalized intermediates, expectations rise for transparency in documentation, clear shelf life projections, and actionable safety data tailored for real research environments. The depth of technical partnership becomes a true selling point.

    Integrating Into Automated and Flow Synthesis

    Production teams working on continuous flow or automated synthesis platforms place strict demands on material reproducibility and cleanliness. Over the last year, researchers integrating 2-Fluoro-4-Cyanobenzyl Bromide into automated modules have reported consistent dosing without line blockages, attributable to controlled particle sizing and careful exclusion of dust-like fines. This allowed them to push beyond batch paradigms, achieving higher throughput in both library synthesis and small API campaigns. In internal trial runs, process engineers confirmed reduced reactor fouling compared to less refined grades or alternative functionalized bromides. For those running 24/7 pilot lines, this translates directly to less downtime and predictable maintenance.

    Finding Solutions for Synthesis Challenges

    Every chemist has battled a tough benzylation reaction or coped with overalkylation byproducts. The double-functionalized ring on our 2-Fluoro-4-Cyanobenzyl Bromide consistently delivers selectivity during stepwise alkylation, avoiding many headaches associated with unplanned side products. In the hunt for novel ligands or CNS-active compounds, both the fluorine and cyano group open clear new synthetic avenues. Years in custom synthesis taught us the value of anticipating not only what chemists want now but what their next demands will be. Our ability to supply well-characterized intermediates meeting tight timelines often gives emerging projects the push needed to move beyond concept to tangible results.

    Addressing Remaining Barriers in Adoption

    Some hesitate to switch from their legacy intermediates or perceive functionalized aromatics as tough to handle. Our approach involves direct consultation with technical teams, sharing practical advice on dissolution, choice of solvents, and reaction conditions. Early collaborations ironed out common sticking points—solubility in mixed polar/apolar solvents, temperature management, and downstream deprotection. The result: more predictable, cleaner runs, with less material lost to pilot-scale optimization. Customers focusing on green chemistry principles have shared valuable strategies for limiting halogenated waste or working at lower concentrations, feedback that feeds directly into our next development efforts.

    A Track Record in Secure, Scalable Supply

    Raw material bottlenecks or inconsistencies in specialty production can upend even well-planned research. With this in mind, we’ve invested in both capacity expansion and contingency sourcing for precursors. Over several cycles, successful scaleups have kept project milestones on track even during market volatility. Feedback from process managers points to reliable logistics and shelf-ready packaging as much as actual product performance. From five kilo runs to several hundred kilos, documented order histories support repeatable, traceable procurement cycles.

    Building the Future with Smarter Intermediates

    It’s clear from feedback and continued innovation that 2-Fluoro-4-Cyanobenzyl Bromide has shifted the landscape for anyone building on benzyl halides. Instead of incremental improvements built around simpler molecules, teams can leap ahead by taking advantage of well-chosen dual substitution. Advanced molecular design calls for smarter, not just more, intermediates. Our team’s experiences—troubleshooting scaleups, refining purification protocols, and partnering with both large and small clients—prove that the evolution of chemical manufacturing must respond to rising complexity, tight regulatory standards, and accelerated project cycles.

    Partnering on Tomorrow’s Synthetic Challenges

    What the last decade has reinforced is how the next breakthrough, whether in drug discovery or material science, often hinges on fast access to the right intermediates. The value from 2-Fluoro-4-Cyanobenzyl Bromide emerges at every link in the chain. R&D scientists repeatedly emphasize the time saved through smarter choices upstream, allowing downstream innovations to materialize sooner and with less risk. Listening to concerns, sharing technical insights, and acting on real-world feedback—not just abstract product data—make the difference. This is the continuing promise of advanced chemical manufacturing.