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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 | 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. |
Applications of 2-Fluoro-4-Cyanobenzyl Bromide in Industrial ManufacturingAs 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 SynthesisLeading 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
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2. Pharmaceutical Intermediate ManufacturingPharmaceutical 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
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3. Specialty Material Monomer ProductionProducers 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
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4. Liquid Crystal Compound ManufacturingProducers 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
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.