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2-Bromo-5-Fluoroanisole

    • Product Name 2-Bromo-5-Fluoroanisole
    • Alias 5-Fluoro-2-bromoanisole
    • Einecs 401-060-3
    • 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

    448864

    Name 2-Bromo-5-Fluoroanisole
    Cas Number 136776-37-3
    Molecular Formula C7H6BrFO
    Molecular Weight 205.03 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 207-209°C
    Density 1.568 g/cm3
    Refractive Index 1.540
    Purity Typically ≥98%
    Smiles COC1=CC(=CC=C1Br)F
    Inchi InChI=1S/C7H6BrFO/c1-10-7-3-2-5(9)4-6(7)8
    Solubility Insoluble in water; soluble in organic solvents
    Storage Temperature Store at room temperature
    Synonyms 2-Bromo-5-fluoro-1-methoxybenzene

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

    Packing & Storage
    Packing The 2-Bromo-5-Fluoroanisole comes in a 25g amber glass bottle, tightly sealed, with hazard and handling labels for laboratory use.
    Shipping 2-Bromo-5-Fluoroanisole is shipped in sealed, airtight containers to prevent leakage or contamination. It is classified as a hazardous material and should be handled with appropriate safety measures. Shipping complies with regulations such as IATA, IMDG, and DOT, ensuring safe transport. Proper labeling and documentation are provided for traceability and safety.
    Storage 2-Bromo-5-fluoroanisole should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. Proper chemical storage cabinets should be used, and the compound should be kept at ambient temperature. Ensure appropriate labeling and restrict access to trained personnel only.
    Application of 2-Bromo-5-Fluoroanisole

    Applications of 2-Bromo-5-Fluoroanisole in Industrial Manufacturing

    2-Bromo-5-Fluoroanisole is a critical halogenated aromatic intermediate used by leading chemical, pharmaceutical, and agrochemical manufacturers. The following industrial application scenarios detail the compound’s integration across core production tracks, specifying compliance requirements, usage guidelines, common process steps, and resulting end products.

    1. Pharmaceutical Active Ingredient Intermediates

    Pharmaceutical manufacturers utilize this compound for the synthesis of select heterocyclic intermediates, especially in API routes for oncology and CNS pipeline molecules. The electron-withdrawing bromine and fluoro substituents facilitate regioselective cross-coupling during key palladium-catalyzed Suzuki or Buchwald-Hartwig reactions. Batch formulation typically incorporates the compound into semi-continuous synthesis steps alongside protected amines or boronic acids, with in-process controls set for halide content and aromatic purity. The downstream validation protocols demand high reproducibility for scalability into cGMP-compliant drug substance production.

    Industry compliance standards

    • ICH Q7 and cGMP (Current Good Manufacturing Practice) for API production
    • USP, Ph. Eur. monographs for intermediate quality (where applicable)
    • FDA 21 CFR Part 211 process requirements
    • Regulatory agency impurity profiling (e.g., FDA, EMA)

    Typical usage ratio

    • 0.10–1.25 molar ratio relative to key substrate, adjusted as per target molecular complexity and reaction yield optimization

    Downstream process integration

    • Introduced post-initial aromatic core formation, prior to amination or coupling
    • Used in controlled halogen-metal exchange or cross-coupling steps
    • Purity and residual halide testing in final intermediate lots

    Final product types

    • CNS-active small molecule APIs (e.g., fluorinated benzodiazines)
    • Brominated kinase inhibitor intermediates
    • NCE (new chemical entity) generation for clinical trial supply
    • Patent-protected intermediates for oncology/antiviral APIs

    2. Crop Protection Synthesis (Agrochemical Intermediates)

    Agrochemical producers employ this aromatic ether as a building block for fluorinated phenoxy herbicides or fungicides. The precise halogenation profile allows for targeted O-alkylation or further functionalization, yielding intermediates required for selective weed control or disease management actives. Integrators apply robust raw material qualification and ensure strict control of residual starting material during the synthesis of active ingredient precursors.

    Industry compliance standards

    • FAO/WHO specifications for active ingredient synthesis
    • ISO 9001–based quality management for agrochemical manufacturers
    • REACH registration for raw material import/export in the EU
    • Local environmental emission standards for halogenated intermediates

    Typical usage ratio

    • 0.20–0.85 molar equivalents to ester or etherification partners, adjusted according to catalytic system and formulated actives’ yield

    Downstream process integration

    • Dosed in the early synthetic stages for fluorophenoxy or brominated aromatic core construction
    • Subsequent hydrolysis, oxidation, or coupling reactions for final active synthesis
    • Residual solvent and halide monitoring in intermediate storage

    Final product types

    • Fluorinated herbicide actives (e.g., phenoxyacetic acid derivatives)
    • Aromatic fungicide key intermediates
    • Precursor compounds for next-generation crop protection molecules
    • Developmental agrochemical test samples for pilot trials

    3. Electronic Chemicals Manufacturing

    Advanced materials producers apply this compound in the design of aryl ether monomers for functional polymers, particularly in organic electronic and display applications. The specific placement of bromine and fluorine on the aromatic ring supports precise control over polymer electronic properties in dielectric films, OLED materials, or sensor substrates. Formulators incorporate the compound at the monomer synthesis stage, with emphasis on achieving high-purity, low-metal content suitable for electronic grade requirements.

    Industry compliance standards

    • JEDEC (Joint Electron Device Engineering Council) standards for material purity
    • IEC 61249-2-21 for halogen-free and fluorinated compounds in electronics
    • RoHS (Restriction of Hazardous Substances Directive) for downstream finished electronics
    • Internal QC for trace metal and ionic contamination

    Typical usage ratio

    • 5.0–15.0 wt% of total monomer mix for functionalized polymer synthesis, optimized per batch requirements

    Downstream process integration

    • Serves as an aryl ether precursor in the monomer blend for condensation polymerization
    • Direct input in Suzuki or Stille cross-coupling polymer backbone reactions
    • Purity assay and halogen analysis as part of incoming QC

    Final product types

    • High-performance dielectric polymers for electronic displays
    • OLED intermediate materials
    • Functional fluorinated coatings for sensors
    • Custom halogenated building blocks for electronic testing

    4. Fine Chemicals and Specialty Aromatic Synthesis

    Producers of fine chemicals and custom synthesis laboratories utilize this compound as a tailored halogenated aromatic starting material for fragrance ingredients, advanced dyes, and certain antimicrobial agents. The unique substitution pattern allows for selective demethylation, formylation, and condensation reactions, yielding specialty products with defined aromatic character. Industrial users control for side-product minimization and consistent quality, integrating advanced analytical verification at intake and post-reaction workup.

    Industry compliance standards

    • ISO 9001:2015 for fine chemical batch traceability
    • IFRA (International Fragrance Association) restrictions for relevant intermediates
    • EN 71-3 (for aromatic dye precursors used in consumer products)
    • DOT and ADR transport regulations for halogenated chemicals

    Typical usage ratio

    • 2.0–10.0 mol% of total reactant charge, with tuning based on desired end-fragrance or chromophore intensity

    Downstream process integration

    • Feeds into demethylation or formylation steps for final aromatic modification
    • Used in condensation pathways for dye precursor assembly
    • Byproduct monitoring and neutralization according to specialty product specification

    Final product types

    • Fluorinated aromatic fragrance ingredient intermediates
    • Specialty dye molecules for plastics and textiles
    • Antimicrobial aromatic compounds
    • Custom research chemicals for third-party development
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    Certification & Compliance
    More Introduction

    2-Bromo-5-Fluoroanisole: Building Better Chemistry One Molecule at a Time

    In our chemical production facility, the synthesis of 2-Bromo-5-Fluoroanisole stands as one example of where precision meets practical needs. With a molecular formula of C7H6BrFO, and a CAS number of 446-10-6, this intermediate commands a place in our schedule not only for its demand but also for the technical skill involved in its production. Throughout the years in manufacturing, we have learned that details at each step—from raw material handling to finished product isolation—shape the end result, and there is nothing generic about these details.

    What Sets 2-Bromo-5-Fluoroanisole Apart

    Chemists in both research labs and industrial settings ask for this compound because of its unique combination of a bromo and a fluoro group on the anisole ring. This para-fluoro, ortho-bromo substitution pattern rarely comes as an accident in synthetic chemistry; it stems from intentional reactions under controlled conditions. The anisole’s methoxy protection offers chemical stability, which is valuable for further transformations. Unlike more straightforward brominated or fluorinated benzenes, the dual functionalization opens up a menu of coupling reactions, especially in pharmaceutical and agrochemical research.

    In our plant, synthesizing 2-Bromo-5-Fluoroanisole is not a one-size-fits-all process. We manage precise halogenation steps and monitor reactivity closely. Yields hinge on reagent purity, reaction temperature, and the rigor of our separation. Techniques from high-vacuum distillation to column chromatography play a part. Each batch logs a purity profile—commonly reaching 98% or better, as verified by gas chromatography and NMR confirmation. Impurity levels, moisture content, and physical appearance (typically a clear to light yellow liquid) stay under tight scrutiny by our QA team, and every in-process sample traces back to our commitment not just to quality, but authenticity.

    Harsh reaction conditions, stray light exposure, and improper storage each threaten the integrity of halogenated anisoles. Over the years, we have learned to control for these variables. A minor slip in temperature or exposure may tilt the product ratio or generate by-products, so continuous feedback from the lab floor can guide course corrections even before the analytical data rolls in. Trained eyes and practiced hands spot the subtle signs—color, aroma, density changes. Each experience builds sharper instincts over time.

    Applications in Synthesis: Why Manufacturers and Chemists Choose This Molecule

    The requests we get for 2-Bromo-5-Fluoroanisole often come with a story. Sometimes, a client is developing a new series of targeted kinase inhibitors; other times, it is an agricultural company exploring novel herbicide scaffolds. The molecule’s unique substitution pattern supports Suzuki, Stille, and Buchwald-Hartwig couplings. For these chemistries, the presence of both bromo and fluoro groups presents an advantage: the bromo affords a labile site for metal-catalyzed cross-coupling, and the fluoro tunes electronic properties, affecting both reactivity and the biological profile of the resulting compounds.

    Many substitutes exist—other fluoroanisoles, mono-brominated anisole, or isomeric bromo-fluoro compounds—but their reactivity and downstream functionalization are not equal. For example, 2-Bromoanisole lacks the electronic influence imparted by the fluorine. On the other hand, 5-Fluoroanisole does not offer a suitable handle for Pd-catalyzed reactions common in medicinal chemistry. 2-Bromo-5-Fluoroanisole nestles into synthesis plans, letting chemists design around both sterics and electronics, expanding into combinatorial chemistry or advanced lead optimization.

    Direct users—research chemists and process development teams—articulate these differences based on hands-on results. For some, the precise substitution lets them achieve regioselectivity unattainable with other monosubstituted anisoles. For others, it is the spectral “fingerprint” of our product—an NMR set that matches tightly to reference spectra and displays consistency. Researchers often provide feedback, and over decades of operation, this dialogue has shaped incremental improvements to our process, from altering solvent selections to slight tweaks in workup temperature.

    Handling, Storage, and the Practical Side of Supply

    Anyone handling bromo-fluoro derivatives knows that shelf life and transport conditions affect performance in downstream applications. In our storage warehouses, we avoid metal containers or reactive plastics. Temperature control remains a daily priority—not just for compliance, but for preserving volatile organics. Old habits from years on the job—checking seals, rotating stock, monitoring for odor or slight yellowing—keep product integrity high. Our experience has shown that even trace moisture alters reactivity, especially in air- or moisture-sensitive transformations.

    Shipping to neighboring labs or across continents, regulations pose logistical obstacles. ADR, IATA, and IMDG guidelines all impose restrictions. Our shipping department’s expertise comes from hands-on familiarity with chemical codes and routine dialogue with regulators, not just rulebooks. With bromo-fluoro anisoles, packaging, labeling, and documentation ask for thoroughness. We audit our practices regularly, and never treat these tasks as paperwork alone—each step minimizes risk for recipients and handlers downstream.

    Comparing to Other Anisole Derivatives: Practicalities, Not Just Structures

    A scientist may study structures on a page, but synthetic experience shapes what chemicals achieve in practice. 2-Bromoanisole and 4-Fluoroanisole—both widely available—fail to deliver the same cross-coupling versatility as 2-Bromo-5-Fluoroanisole. Their reactivity, ease of purification, and downstream transformations diverge, sometimes in subtle but important fashion. In one customer’s case, moving from a mono-substituted anisole to 2-Bromo-5-Fluoroanisole nearly halved the number of steps needed to access the target scaffold, tightening project timelines.

    There’s also a question of scale. We know that on paper, lab reactions scale simply by multiplying weights and volumes, but our production stories show that this rarely works in practice. 2-Bromo-5-Fluoroanisole’s dual reactivity poses challenges—side products can multiply with scale. Our reactor operators flag off-normal frothing and exotherms early, sometimes improvising agitation schemes or adjusting cooling rates in real time. This on-the-ground vigilance, born from years of plant work, prevents costly failures, especially when producing metric tons for a custom contract.

    Consistency and Quality: Lessons From the Plant Floor

    Guidelines don’t guarantee reliability, but practice, repetition, and close process observation have taught us what quality looks like. Visual checks—clarity, absence of particles, proper coloration—matter as much as the cold data from our chromatographs. Batch variation has dropped as we standardized filtration, drying schedules, and product transfers within inert environments. Our process chemists engage in troubleshooting that goes beyond the standard playbook. If a reaction stalls, or impurities climb by a tenth of a percent, we perform root cause searches that connect maintenance logs, supplier quality, and subtle equipment wear.

    Future buyers often ask about batch-to-batch reproducibility, and our response comes backed by real traceability. Tens of years’ worth of retained samples let us roll back the chain of custody, linking every container’s journey through the plant. When new regulatory requirements appear, or when a customer experiences a process deviation, these samples inform necessary adjustments. Our continuous investment in on-site analytical instrumentation—GCMS, NMR, LC—shortens turnaround and keeps product on-spec, across each shipment.

    We run pilot batches jointly with partners developing scale-up routes. Process changes—say, a switch to greener solvents or a new workup protocol—pass through staged validation. In these collaborations, we gain perspective on how the product behaves outside our walls, infusing field feedback into every improvement effort. In the case of 2-Bromo-5-Fluoroanisole, one pharmaceutical customer needed stringent documentation of trace contaminants for registration; joint review led us to upgrade filtration and distillation stages, cutting impurity levels to below 0.1%.

    Industry Demand and Shifts in Usage Patterns

    Requests for 2-Bromo-5-Fluoroanisole have grown in tandem with the rise of targeted pharmaceuticals and specialty agrochemicals. Each spike in demand usually tracks to a new discovery campaign or the advance of a candidate molecule toward scale-up. We keep an ear to the ground through both sales channels and supplier reports. In the past, surges in interest have led to supply bottlenecks of precursor chemicals—fluorinated benzenes being the most unpredictable. Our solution usually involves forward contracting and qualifying backup suppliers. Experience in forecasting needs and buffer inventory management steers us through these cycles more smoothly than a simple-in, simple-out inventory plan.

    One pattern is clear: chemical portfolios among our customers are getting more diverse, with structurally complex molecules replacing simpler ones. 2-Bromo-5-Fluoroanisole, with its twin points for functionalization, gives research teams a shortcut into more elaborate frameworks. Downstream, this means customers risk less time on re-optimization if one synthetic avenue closes. From our conversations with process development leaders, it’s clear they value the ability to try alternate cross-couplings without the overhead of resourcing a wholly new starting material.

    Within the research community, the molecule’s uptake marks a shift toward modular synthesis—the trend toward “build and branch” pathways rather than single-step substitutions. As demands for patient-specific therapies or “greener” syntheses rise, 2-Bromo-5-Fluoroanisole’s functional group arrangement enables selective transformations without extensive protection and deprotection cycles. In essence, our job grows less about moving drums and more about supporting creative synthetic design—whether in small discovery scale or larger development campaigns.

    Sustainability Concerns and Process Improvements

    Environmental scrutiny over halogenated aromatics shapes our efforts to keep waste low and recover solvents. Brominated and fluorinated compounds bring concerns about toxicity, persistence, and regulatory monitoring. Early in our years of production, we handled waste streams with external vendors exclusively. Hard experience—not just regulatory pressure—pushed us to overhaul: now we recondense, neutralize, and recycle as much as possible. By stripping spent solvents and reusing them after purification, we lower both raw material costs and emissions, lessons learned in the reality of tight margins and regulator visits.

    Among the biggest improvements has been an upgrade to our distillation network, which permits us to separate, clean, and reuse fractioned solvents without loss in yield or product quality. We modularized our reaction vessels for faster switchover and lower cross-contamination risk, drawing lessons both from on-the-ground incidents and ongoing customer audits. Each improvement arose from partnership—internal teams, analysis of customer comments, or new regulations driving the need for traceability at ppm levels. Responsibility, in our experience, isn’t performed out of obligation but because every operator wants to know their efforts mean a safer, smarter facility.

    For 2-Bromo-5-Fluoroanisole, waste minimization also impacts the control of air and water emissions. Brominated streams undergo multilayer filtration and neutralization to eliminate accidental releases. Our team’s investment in automation, real-time LEL monitoring, and careful logs add traceability. Each batch drives a record of compliance not just to satisfy outside auditors but to assure ourselves and our partners that these compounds can be manufactured with minimal environmental impact.

    Skill, Knowledge, and the Edge From Experience

    No process, no matter how polished in the SOP, runs itself. What sets apart true manufacturing from simple contract filling is experience: the quiet sum of many cycles, dozens of conversations, and nights spent making sense of why a batch didn’t go as planned. With 2-Bromo-5-Fluoroanisole, these skills matter—balancing halogen substitutions, dialing in the right reactivity, catching the faintest impurity through experience and a trained nose as much as any instrument’s readout.

    In comparison to resellers or distributors, the direct manufacturer has unique insights: the feel of raw materials, the “look” of a solution as it refluxes, the lessons of a hundred formed crystals. We pass this perspective on to our customers, not from a manual, but drawn from memory, conversations, and the quiet accumulation of trust. For those seeking more than a simple off-the-shelf intermediate, our doors—and ears—remain open, recognizing that molecules do more than fill bottles: they drive discovery, shape industries, and benefit from each hand that shapes them.

    Across years of contract synthesis, scale-up, and custom work, we have come back again to the value of long-term relationships—both inside our plant and with our clientele. Chemists and process experts on both sides eventually move beyond transactional exchanges to collaborative problem-solving. Sometimes it means revisiting old data, other times redesigning process flow, or troubleshooting a tricky impurity or spectral anomaly. The product—2-Bromo-5-Fluoroanisole—may stay constant in formula, but the ways we deliver value evolve.

    The Future of 2-Bromo-5-Fluoroanisole and Our Approach

    As regulatory landscapes shift and research priorities head toward complexity and specificity, intermediates such as 2-Bromo-5-Fluoroanisole take on new roles. The molecule now surfaces in clinical candidate syntheses and advanced material research, reaching applications that a decade ago were mostly in basic research. We adapt by investing in up-to-date analytics, continuous training, and persistent dialogue with both technical and commercial partners. Every improvement we make emerges not from abstraction, but from solving real-world challenges—reducing waste, cutting cycle times, or troubleshooting reactions where milligrams count.

    Staying grounded in the work of real chemical manufacturing—not just moving intermediates, but continually refining them—gives us purpose. Our experience with 2-Bromo-5-Fluoroanisole stands as evidence: the market’s needs for high-purity, reproducible, and versatile building blocks demand a level of engagement only true production experience can offer. Taking pride in each batch, we remain committed to making not just chemicals, but future possibilities, one molecule at a time.