Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales7@sinochem-nanjing.com 3389378665@qq.com
Follow us:

1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene

    • Product Name 1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene
    • Alias 1-Bromo-2-fluoro-4-(trifluoromethoxy)benzene
    • Einecs 629-653-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    331607

    Productname 1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene
    Casnumber 146137-98-6
    Molecularformula C7H3BrF4O
    Molecularweight 259.99
    Appearance Colorless to pale yellow liquid
    Boilingpoint 151-154 °C
    Density 1.762 g/cm3
    Purity Typically ≥98%
    Refractiveindex 1.474
    Smiles C1=CC(=C(C=[C]1OC(F)(F)F)F)Br
    Inchi InChI=1S/C7H3BrF4O/c8-4-1-2-6(13-7(10,11)12)5(9)3-4/h1-3H

    As an accredited 1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, tightly sealed with a screw cap, labeled with chemical name, CAS number, and hazard warnings.
    Shipping **Shipping Description:** 1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene is shipped in tightly sealed containers under cool, dry conditions. It should be labeled as a hazardous chemical, handled by trained personnel, and transported according to local, national, and international regulations for chemicals, ensuring protection from moisture, heat, and physical damage during transit.
    Storage **1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene** should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Keep container tightly closed when not in use. Always follow appropriate chemical safety protocols and store at recommended temperature, usually at or below room temperature.
    Application of 1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene

    Applications of 1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene in Industrial Manufacturing

    1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene serves as a strategic intermediate across specialized chemical industries, where demand for precision fluorinated and brominated aromatic compounds continues to rise. As a direct manufacturer, we ensure strict process control for consistency and purity, supplying downstream operations that require reliable performance in their complex syntheses.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient Synthesis

    This compound functions as a build block in the multistep synthesis of fluorinated and trifluoromethoxy substituted APIs, especially in central nervous system therapeutics and oncology candidates. Medicinal chemistry groups utilize it for introducing specific halogen patterns, enabling essential structure–activity relationship exploration. Our material fits critical stages following initial ring construction, before final functionalization steps, helping downstream partners achieve high target selectivity. Stringent residual solvent and heavy metal controls are applied throughout shipment and storage, guaranteeing compliance for further cGMP processing by end customers.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapter <795>, <797> residual solvent and elemental impurity requirements
    • REACH and TSCA registration (substance premanufacture notification)
    • Ph. Eur. monograph raw material screening requirements

    Typical usage ratio

    • Employed as a key intermediate, loading rates range 1:1 to 1:5 molar versus nucleophile or aryl coupling partners
    • Quantities adjusted based on specific pathway—higher excess used in Suzuki or Buchwald-Hartwig couplings to drive conversion

    Downstream process integration

    • Introduced following initial arene formation, before palladium-catalyzed C–C or C–N cross-coupling
    • Dehalogenation or functional group exchange performed in third or fourth synthetic step
    • Segregated handling under high-purity, nitrogen-purged system in multi-kilogram reactors

    Final product types

    • CNS-active pharmaceutical intermediates
    • Fluorinated kinase inhibitors and tyrosine kinase inhibitor fragments
    • Precursor for PET tracer development
    • Reference standards used by analytical laboratories

    2. Agrochemical Synthesis Intermediate

    Chemical manufacturers apply this material for constructing fluorinated and trifluoromethoxy-containing aromatic rings within modern herbicide and fungicide molecules. The compound’s halogenated character imparts enhanced bioactivity and metabolic stability to the resulting crop protection actives. During integrated manufacturing routes, direct bromination or nucleophilic substitution proceeds after aromatic ether formation, ensuring controlled introduction of the functional moiety under scalable, industrial conditions.

    Industry compliance standards

    • Food and Agriculture Organization (FAO) Specification for Technical Grade Active Ingredients
    • OECD Good Laboratory Practice for test substances
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • ISO 9001:2015 quality management during raw material production

    Typical usage ratio

    • Dosage of 0.8–1.1 molar equivalent in Suzuki-Miyaura or aromatic nucleophilic substitutions against active core fragments
    • Stoichiometry tuned based on scale-up process yields and impurity minimization

    Downstream process integration

    • Added as a halogenated substituent in early to mid-stage process (pre-cyclization or before diazotization)
    • Enters closed loop reactors with robust temperature and pH monitoring
    • Intermediate isolation done prior to final pesticide salt formation stage

    Final product types

    • Trifluoromethoxy-substituted pyrazole herbicide actives
    • Systemic fungicide technical concentrates
    • Precursor molecules for crop treatment R&D
    • Analytical pesticide standard substances

    3. Fluorinated Material for OLED and Electronic Chemicals

    Leading electronics manufacturers use this compound to introduce specialized fluorinated moieties into small molecule semiconductors and display materials, particularly for organic light-emitting diode (OLED) and organic transistor device fabrication. It enables targeted enhancements in electron mobility, chemical resistance, and dielectric strength of final structures. Incorporation occurs through metal-catalyzed cross-coupling with thiophene or aryl cores, integrated under inert conditions with strict trace metal control. Batch release matches specifications required for microelectronic-grade feedstock materials.

    Industry compliance standards

    • IPC-4101B for electronic component raw materials
    • RoHS Directive 2011/65/EU (limiting hazardous substances in electronics)
    • IEC 61249-2-7 for base materials—halogen-free requirements as applicable
    • ISO 14644-1:2015 (cleanroom processing background)

    Typical usage ratio

    • Implemented at 0.5–1.3 molar equivalent during aryl coupling depending on substrate reactivity and end-device molecular weight
    • Adjusted to balance target luminance and desired bandgap in electronic grade synthesis

    Downstream process integration

    • Reacted with polycyclic or heteroaromatic cores at initial polymerization or terminal functionalization step
    • Process carried out in high-purity, solvent-free or ultradry solvent systems under cleanroom conditions
    • Material subjected to multi-step purification before use in display fabrication

    Final product types

    • OLED blue and green emitters
    • Small molecule semiconductors for display drivers
    • Dielectric thin films for flexible electronics
    • Photovoltaic charge transport materials

    4. Intermediate for Specialty Fluorinated Polymer Synthesis

    The compound acts as an aromatic monomer precursor in the synthesis of high-value fluoropolymers and specialty resins. Polymer chemists employ it to impart unique chemical resistance and low surface energy by introducing combinations of bromine, fluorine, and trifluoromethoxy substituents onto arene-based backbones. It typically enters processes during secondary monomer formation, well before polycondensation or radical polymerization stages. Downstream users emphasize control in trace halide and oligomer content, ensuring reliable polymer branching and consistent mechanical properties.

    Industry compliance standards

    • ASTM D5630-13 (loss on ignition for halogenated polymers)
    • UL 94 (flammability rating for final polymers)
    • ISO 9001:2015 and 14001:2015 for controlled polymer manufacture
    • EPA TSCA Inventory listing

    Typical usage ratio

    • Utility at 2–10% by weight of monomer charge, depending on the end-use and copolymer composition
    • Proportion selected after trial batch evaluation to optimize polymer physical characteristics

    Downstream process integration

    • Used in monomer pre-functionalization before full polymerization cycle
    • Introduced as a feed to solution or suspension polymerization reactors under nitrogen
    • Purified and dried for direct addition to pre-polymerized mass in downstream mixing or extrusion

    Final product types

    • High-performance fluorinated resins
    • Coatings for anti-fouling or electronic substrate layers
    • Fluoropolymer films with UV and chemical resistance
    • Modified specialty elastomers for chemical processing equipment
    Free Quote

    Competitive 1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene: A Manufacturer’s Perspective

    Purpose Behind Our Work

    Every product we create at our facility is rooted in real-world demands and shaped by the continual feedback that comes from those who use advanced intermediates daily. 1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene represents not just a specialty halogenated aromatic but a calculated choice in the modern chemist’s toolkit. The reasons our team remains committed to this compound draw from our years of experience tackling problems at the bench and in plant-scale synthesis.

    Molecular Details and Consistency Above All

    Our process for synthesizing 1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene places a premium on controlled reactivity and clean conversion. Each batch is tracked through to the finished product, and we routinely keep analytical data for GC, NMR, and MS on file. Chemically, this compound consists of a benzene ring carrying bromine and fluorine on adjacent carbons, with a trifluoromethoxy substituent set at the para position. The configuration of these groups affects both its electron distribution and subsequent patterns of reactivity. Small changes in handling or impurity profiles tend to show up downstream, so we apply a hands-on QC approach. By steering clear of shortcuts and maintaining multi-stage verification, we deliver stable lots suited for scale-up or sensitive applications.

    Our internal specification follows years of experience responding to questions from medicinal chemists, agrochemical innovators, and materials scientists. We set our typical purity threshold at over 98 percent by GC, though we often reach 99 percent. We avoid using stabilizers or blending agents because side reactions can spiral out of control during functionalization if unexpected residues crop up. Consistent melting range and clear spectral signatures help our customers avoid unplanned purification steps.

    Application-Driven Manufacturing Decisions

    We began regular production of this substituted aromatics after several partners in fluorine chemistry described bottlenecks in late-stage diversification. Classic aryl bromides have long played a central role in coupling reactions, but selectivity issues often arise when a molecule contains both electron-withdrawing and electron-donating groups. The trifluoromethoxy group confers distinct reactivity over simpler trifluoromethyl analogs. Bonds close to the OCF3 moiety show enhanced cross-coupling activity, especially with palladium catalysts.

    Our involvement with academic and industrial medicinal chemistry labs revealed that customers value the dual halogenation pattern for directed ortho metalation and regioselective transformations. The bromine acts as a versatile handle for palladium-catalyzed Suzuki, Buchwald–Hartwig, or Stille reactions. Meanwhile, the fluorine can resist metalation or undergo selective aromatic displacement, which broadens synthetic options. Customers leveraging this product for candidate library synthesis or SAR studies often note successful site-selective transformation without requiring multiple protection–deprotection cycles.

    Compared with more commonly available aryl bromides or trifluoromethoxybenzenes lacking ortho-fluorine, this molecule offers a balance of lability and stability. Where un-substituted para-OCF3 benzenes may give ambiguous regioselectivity during nucleophilic attack, this particular arrangement defines the reactive sites while minimizing side reactions.

    Troubles Faced and Lessons Learned on the Plant Floor

    Over the years, we have learned a few things the hard way. Multi-halogenated aromatics like 1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene create their own operational puzzles. Controlling the sequence of halogenation during synthesis means optimizing for temperature, solvent polarity, reagent grade, and reaction timing. Early batches taught us that minor solvent contamination or humidity changes could lead to over-bromination, ring rearrangement, or even decomposition of the trifluoromethoxy group. These lessons pushed us to invest in precise water removal, closed-system feedstocks, and high-grade reagents. Our reactors are lined with corrosion-resistant alloys, and batch records reflect a sensitivity to minor fluctuations in ambient air.

    We have also seen how impurities—even those hiding below the visible detection limit—can poison catalysts, reduce yields, or contribute to inhomogeneity in subsequent steps. Our operators clean glassware and lines far beyond standard levels to keep cross-contamination to a minimum. To help groups working at the R&D or kilo-lab scale, we supply SDS and full analytical profiles without delay so process adaptation occurs with full transparency.

    Finding the Sweet Spot: Why Customers Come Back

    We see the greatest demand from innovators in pharma and crop protection, especially groups pursuing robust C–C or C–N coupling strategies. Both the electronic and steric effects created by our compound shape its use in advanced synthesis. Medicinal chemists—often under pressure to test new substituent combinations on core scaffolds—tell us they return to this specific halogen layout because it reduces the need for later-stage troubleshooting. Our contacts in materials science leverage the strong electron-withdrawing character of both the OCF3 and fluorine for tuning optical and surface properties of polymers and liquid crystals.

    One aspect separated our product from others: our sustained commitment to keeping microimpurities and byproduct formation as low as technically possible. We learned that in iterative syntheses or automated parallel library runs, even trace decomposition byproducts can affect SAR interpretation or screening results. By listening directly to customer feedback, we adjusted purification, invested in online monitoring, and fine-tuned crystallization to consistently deliver a reproducible intermediate.

    How This Compound Stands Apart

    Much of the conversation with customers centers not only on raw purity but also on reactivity and performance in target transformations. Many commodities or generics contain mixed halogen loads or suffer from residual solvents. Our product, built from the ground up with tight process controls, gives not just high assay but actual fit-for-purpose suitability. With alternatives on the market often showing less predictable coupling rates or yielding unexpected side products, we document our lots with detailed chromatograms and test coupons for verification. Some competitors' supplies carry high water content, leading to hydrolysis or deactivation during amination or cross-coupling. We keep residual water tightly controlled, and every drum is packaged and sealed under inert atmosphere as a rule, not as an afterthought.

    Feedback from process development teams across three continents highlights faster throughput and fewer column purification steps compared to less refined sources. One team replaced their prior supplier after repeated problems with color impurities and inconsistent halogen balances. Our team responded by sharing actual processing notes and scaling data, not just a paper specification or one-off certificate of analysis. This style of transparency has reduced time spent troubleshooting and improved project timelines for those pushing toward IND filings or new formulation ventures.

    Supporting More Than Just Delivery

    The role of a chemical manufacturer extends well beyond just filling drums and labeling containers. Our chemists regularly support direct application needs, fielding calls about novel catalyst systems, solubility questions, or ways to reduce residual metals. Early-stage customers sometimes share unexpected findings—such as reactivity with new ligands or solvents. We use this feedback loop to refine our next manufacturing cycle. Rather than hiding behind template communications, our team engages in open exchanges to help users avoid pitfalls and maximize output.

    We also back our supply with the technical “why” behind each batch. With more groups running high-throughput screening and advanced analytics, real knowledge transfer on side products, long-term storage, and appropriate transfer lines has become just as important as the molecule itself. This approach aligns technical stewardship with day-to-day operations, helping others build confidence in their own output. For us, the end goal is not simply matching a molecular structure, but supporting the total lifecycle of each project using our compound.

    Sustainability, Safety, and the Road Ahead

    The push for more responsible chemistry shapes our own plant operations just as much as it influences our customers. While 1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene requires careful handling due to both reactivity and volatility, we continuously review exposure controls and engineering updates to minimize emission or waste. Investing in closed-loop solvent recovery and air filtration, we aim for both compliance and true risk reduction. In practical terms, this means more efficient use of reagents, lower worker exposure, and more reliable shipment profiles for our buyers.

    We make a point of liaising with downstream handlers and waste processors. Our support does not drop off once a product leaves the plant. Over the last five years, we have worked to map the breakdown and environmental fate of byproducts, sharing this information directly with partners looking to optimize EHS protocols in their own organizations.

    Continuous Refinement in a Competitive Landscape

    Improvement remains a non-stop project for us. Each feedback loop raises the bar on what the next batch will deliver. Our partnerships span more than simple supply contracts—technical exchanges keep us connected to emerging synthetic trends, safety requirements, and analytical advances. Many contemporary projects—especially in advanced drug discovery—demand flexible thinking and a willingness to adapt. We regularly cross-check our synthesis parameters against new literature, in-house data, and supplier updates to sustain a competitive edge.

    Handling an advanced aromatic intermediate requires discipline in everything from raw material sourcing to product isolation and packaging. We train our operators directly, sharing knowledge on real-world problems encountered at every scale. Tiny lapses in the routine—be it a pump seal, a line rinse, or a misread sensor—can show up as headaches much later for our customers. For us, quality in 1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene reflects every link in this chain, from first reagent feed to final closure.

    Community, Collaboration, and the Future of Halogenated Aromatics

    We do not operate in isolation. Our work in complex aromatic intermediates draws on ideas, critique, and even direct troubleshooting advice from those we serve. Open doors and regular dialogue, whether over a video call or in project site visits, mean that with each run, the compound leaving our gates better supports the complicated pathways and performance demands customers expect.

    Into the future, we see steadily rising expectations for higher selectivity, cleaner side product profiles, and both upstream and downstream sustainability. With regulators focusing closely on process byproducts and end-of-life environmental impact, our team remains committed to steady updates, new analytical validation, and real responsiveness. Our entire operation—from lab development through to logistics—relies on applying experience, honesty, and hands-on action at every step.

    Direct Results for Real Users

    We see the application world for this molecule split evenly between targeted coupling, library diversification, and input for next-generation materials. Process chemists value short, predictable reaction times and resilient profiles in both pilot and scale-up. Development teams rely on accurate, timely screening data to make go/no-go decisions for new synthetic directions. Formulation scientists focus on contaminant-free benchmarks, which direct the packing and post-reaction workups. The smallest details—trace acids, excess moisture, or even packaging material—compound into real consequences if ignored. Our ongoing investment in those details keeps the path clear for both breakthrough applications and reliable routine runs.

    We take pride in delivering not just a product but a considered, responsive partnership. Production is not a one-way street; technical advice and post-sale support matter every bit as much. Ongoing exchange with those closest to application keeps standards precise and innovation shared. That cycle of engagement, hands-on learning, and outcome-focused detail defines what we offer—and why our 1-Bromo-2-Fluoro-4-(Trifluoromethoxy)Benzene stands out in practical use.