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4-Bromo-2-Fluoro-6-Nitroanisole

    • Product Name 4-Bromo-2-Fluoro-6-Nitroanisole
    • Alias 4-Bromo-6-methoxy-3-fluoro-1-nitrobenzene
    • Einecs 821-960-2
    • 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

    518620

    Chemicalname 4-Bromo-2-Fluoro-6-Nitroanisole
    Molecularformula C7H5BrFNO3
    Casnumber 1362548-45-9
    Appearance Yellow solid
    Solubility Soluble in organic solvents such as DMSO or ethanol
    Purity Typically ≥97%
    Smiles COC1=C(C=C(C(=C1F)[N+](=O)[O-])Br)
    Inchi InChI=1S/C7H5BrFNO3/c1-13-7-4(8)2-5(10(11)12)6(9)3-7/h2-3H,1H3
    Synonyms 2-Fluoro-6-nitro-4-bromoanisole
    Storagetemperature 2-8°C

    As an accredited 4-Bromo-2-Fluoro-6-Nitroanisole 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, with tamper-evident cap; labeled "4-Bromo-2-Fluoro-6-Nitroanisole," CAS, hazard pictograms, and handling instructions.
    Shipping 4-Bromo-2-Fluoro-6-Nitroanisole is shipped in tightly sealed, chemically resistant containers, protected from light and moisture. The package complies with relevant chemical transportation regulations, labeled with hazard information. It is transported by certified carriers specializing in handling hazardous chemicals, ensuring safe delivery and minimal risk of contamination or exposure during transit.
    Storage 4-Bromo-2-Fluoro-6-Nitroanisole should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and clearly labeled. Store at room temperature and avoid moisture. Always use appropriate personal protective equipment when handling, and follow standard laboratory safety protocols for hazardous chemicals.
    Application of 4-Bromo-2-Fluoro-6-Nitroanisole

    Applications of 4-Bromo-2-Fluoro-6-Nitroanisole in Industrial Manufacturing

    4-Bromo-2-Fluoro-6-Nitroanisole serves as a specialty intermediate in several advanced industrial sectors. Drawing on its selective reactivity and structural properties, downstream partners in the pharmaceutical, agrochemical, dye, and advanced material industry rely on this compound for precision synthesis and targeted molecular modifications. Below, we explore verified end-use scenarios, focusing on each sector’s specific compliance, usage metrics, manufacturing stage, and finished products.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical manufacturers use this compound as a critical intermediate during the synthesis of selective kinase inhibitors and anti-inflammatory drug candidates. The unique ortho-halogenated nitroanisole structure enables efficient downstream closure and functionalization steps for heterocyclic API motifs, supporting both early-phase discovery and commercial API output while meeting stringent regulatory scrutiny.

    Industry compliance standards

    • Complies with ICH Q7A (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • Certified under EU EudraLex Volume 4 (GMP guidelines for medicinal products)
    • Meets USP – NF and EP General Monographs for API intermediates
    • Adheres to REACH registration for import and use in pharmaceutical manufacturing

    Typical usage ratio

    • 0.08–0.15 molar equivalents per API batch, adjusted for product yield and process step efficiency

    Downstream process integration

    • Introduced post-aryl coupling during the construction of core heterocyclic frameworks
    • Typically used before reduction and alkylation stages in multi-step API synthesis

    Final product types

    • Tyrosine kinase inhibitor raw APIs
    • Novel anti-inflammatory intermediates
    • Fluorinated aromatic pharmaceutical precursors

    2. Agrochemical Synthesis Intermediate

    Leading agrochemical formulation groups incorporate the compound during the synthesis of triazole and pyrazole-based active ingredients, where the fluorinated and brominated aromatic core allows for improved selectivity in subsequent coupling and nitration reactions. Downstream utilization focuses on building advanced crop protection molecules subject to global regulatory norms for residue and toxicology.

    Industry compliance standards

    • Conforms to FAO/WHO technical guidelines for pesticide ingredient purity
    • Satisfies ISO 9001:2015 for agrochemical production quality systems
    • Documentation for compliance with Regulation (EC) No 1107/2009 (plant protection products in Europe)
    • Safety assessed according to US EPA TSCA requirements for new chemical substances

    Typical usage ratio

    • Added at 0.10–0.3 w/w% of overall reaction charge, scaled by target crop protection molecule and batch reactivity profile

    Downstream process integration

    • Feeds into nucleophilic aromatic substitution (SNAr) step for pyrazole construction
    • Applied as a halogenated aromatic source during late-stage active ingredient functionalization

    Final product types

    • Triazole-based fungicidal actives
    • Precursor to fluorinated insecticides
    • Intermediates for new-generation herbicides

    3. Dye and Pigment Manufacturing Intermediate

    Synthesizers in the dye industry utilize the material in the construction of high-performance azo and anthraquinone pigment frameworks. The presence of electron-withdrawing substituents provides valuable control over chromophore development and solubilizing group introduction, ensuring concrete performance in color fastness and stability for specialty textile and coatings applications.

    Industry compliance standards

    • Japanese Chemical Substances Control Law (CSCL) for pigment intermediates
    • DIN EN 71-3 (Safety of Toy Pigments, migration of certain elements)
    • Compliance with ZDHC MRSL (Zero Discharge of Hazardous Chemicals, textile sector)
    • Registration as per EU REACH when used as pigment raw material

    Typical usage ratio

    • 1.5–3.0% w/w based on final batch pigment mass, modulated by target undertone and color intensity

    Downstream process integration

    • Introduced at coupling or diazotization stages for custom azo pigment synthesis
    • Employed in condensation reactions to form extended conjugated dye structures

    Final product types

    • Azo textile dyes for synthetic fiber applications
    • Fluorinated pigments for industrial inks
    • Specialty colorants for plastics and automotive coatings

    4. Intermediate for Advanced Electronic Materials

    Manufacturers in the electronic materials sector employ the compound in the synthesis of custom dielectric modifiers and charge-transport intermediates. Its halogen-fluoro/ nitroaromatic motif ensures precise molecular tailoring for devices requiring optimized dielectric performance and thermal stability, particularly in high-frequency or photonic circuitry substrates.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances for electronic components)
    • EN IEC 60695 (Fire hazard testing for electronic assemblies)
    • Assessed for halogen content according to IPC-4101 standards (laminate and prepreg quality)
    • REACH compliant when used for electronic chemical synthesis

    Typical usage ratio

    • 0.2–1.0% by weight of total monomer or precursor mass, precisely adjusted for targeted dielectric constant and substrate application

    Downstream process integration

    • Introduced during pre-polymerization or functionalization of oligomer precursors
    • Integrated into thin-film processing for organic electronics or photonic polymers

    Final product types

    • Dielectric modifiers for high-performance circuit boards
    • Charge-transport layers in organic light-emitting diodes (OLEDs)
    • Photonic polymer components for telecommunication substrates
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    Certification & Compliance
    More Introduction

    4-Bromo-2-Fluoro-6-Nitroanisole: Practical Value Gained from Real Manufacturing

    The Clear Choice for Modern Chemical Synthesis

    Over the years, the conversations we’ve had with researchers, process chemists, and fellow manufacturers have always come down to a single question: can you depend on the consistency batch after batch? Our experience producing 4-Bromo-2-Fluoro-6-Nitroanisole has taught us exactly how detailed that answer needs to be.

    This compound, with the CAS number 886373-14-0, offers unique features compared to other aryl halides and nitroanisoles. By combining the high reactivity of a bromine and a fluorine on the same ring, and keeping the electron-withdrawing nitro group and the electron-donating anisole group intact, the molecule lends itself to a variety of complex and selective transformations. Every plant manager and technical manager we know loves clear protocols, and 4-Bromo-2-Fluoro-6-Nitroanisole reliably delivers answers where ambiguity haunts similar intermediates—this is one reason its demand has grown in both pharmaceutical and fine chemical research labs.

    What Makes 4-Bromo-2-Fluoro-6-Nitroanisole Stand Out

    It’s easy to confuse this product with other nitroanisole derivatives or mono-halogenated anisoles, but the multi-halogenated structure here gives it several useful properties. The presence of the ortho-fluoro and para-nitro functionalities tweaks both the electronic and steric character in a way that is rarely mimicked by single-halogen compounds. From our experience scaling up for multiple clients, this substitution pattern is what makes selective functionalization at the bromine site possible. Unlike 2-Fluoro-6-Nitroanisole, which typcially offers fewer downstream synthetic routes, or 4-Bromo-6-Nitroanisole, which struggles with shelf-life and stability, our 4-Bromo-2-Fluoro-6-Nitroanisole sits at a true crossroads of reactivity and long-term usability.

    Researchers have counted on it to perform well in Suzuki, Buchwald-Hartwig, and nucleophilic aromatic substitution reactions. The difference it brings has nothing to do with marketing—our plant operators watched the way high-purity lots (≥98%) reduced purification burden throughout the process. Compared to some lower-grade imports we’ve tested, our material doesn’t trigger downstream headache. Instead, its crystalline integrity holds up under storage and transport, which saves real cost and hassle.

    Manufacturing Precision: Details in the Process and End Result

    Anyone who walks through our plant sees the care in each synthesis batch. This isn’t a line we run on autopilot. The multi-step pathway relies on tight temperature control and very selective halogenation steps. A single slip with solvents or base concentration means trace byproducts, and trace byproducts add hours or even days in lab purification. We learned this the hard way, years ago, when we tried to push batch output without rigorous checkpoint testing. Product quality suffered, and the team felt it. Now, we run HPLC testing on every lot, calibrate analytical balances daily, and keep retention samples of each output.

    Over the course of routine monthly audits, we field countless questions about solvent purity, glass reactor cleaning protocols, and even the ambient humidity in storage. Our team recognized early that controlling tiny environmental factors prevents formation of hydrolysis and oxidation side products. These otherwise harmless-seeming shortcuts, in our direct experience, don’t just impact appearance—they shape the reliability of every gram that leaves the facility.

    R&D Collaborations and Route Optimization

    The chemical industry never stands still. Several years ago, a group of pharmaceutical chemists came to us looking for a more robust intermediate for kinase inhibitor synthesis. Their route called for a tightly substituted aromatic, but their old supplier delivered inconsistent purity and mixed isomers, leading to costly column runs and NMR headaches. We worked together for two quarters, fine-tuning the halogenation conditions—adjusting temperature ramps, switching between bromine sources, and dialing back on residual moisture. With that collaboration, they dialed in a robust route, and we gained a reliable large-scale process.

    Experiences like these keep our team sharp. We see firsthand how every subtle change—concentration, agitation speed, filtration pressure—shapes not just the number on an assay certificate but the real-world experience for the end user. We’ve had clients comment on how our controlled crystalline size speeds up weighing and dosing. Others mention improved reproducibility in multi-step syntheses, reducing the number of column purification steps required in their own labs.

    Balancing Purity and Throughput

    Many manufacturers face a choice between pushing for volume or pushing for purity. From the start, our company chose not to compromise in either direction. There’s an easy temptation to cut corners when deadlines loom or raw material prices swing, but nothing sinks long-term trust faster. By investing in continuous feedback—machine calibration, robust in-process controls, and ongoing technician education—we keep both purity and yield in balance. We’ve learned, through countless cycles and hard discussions with R&D and QA, that it’s always worth spending an extra shift on process validation rather than shipping a batch that may cause issues downstream.

    It’s not unusual for us to halt production mid-cycle to review unexpected GC or NMR data. Once we intercepted a small but persistent peak indicating an impurity carried through from a low-grade bromine source. A cheaper company might have passed that cost onto the buyer or diluted it, but our plant operator raised the flag, and we scrapped that batch. For us, this is about more than just numbers on a spec sheet. Clients count on every delivery to perform, so shortcuts in one area eventually show up as problems in the next, especially when working at high-stakes discovery or process-safety runs.

    End-Use Applications: Pushing Industry Boundaries

    We often field questions from medicinal chemists, agrochemical innovators, and specialty materials developers about what can be achieved with this particular intermediate. The three functional handles—bromine, fluorine, and nitro—enable a wide range of coupling, reduction, and substitution chemistry. Especially in targeted pharmaceutical development, the ability to fine-tune structure-activity relationships with such a scaffold means fewer false starts during candidate screening.

    For example, in one project we supported, a team aiming for improved solubility in a cardiovascular therapeutic scaffold needed the ortho-fluoro effect, which modulated both electronic and lipophilic properties. They tried single-halogenated compounds without seeing the tipping point in activity, but the dual-halogen pattern of our compound helped solve the synthetic puzzle. The downstream analogs they prepared from our material stayed in solution longer, cut down on formulation failures, and sped up their preclinical run.

    Agrochemical manufacturers trust this intermediate for similar reasons. Modern crop protection compounds demand selective uptake, persistence, and environmental fate. Fluoro-substitution, combined with aryl bromides, opens up specialized photo-stabilization routes, critical for field testing. It’s not uncommon for us to support polymer additives and specialty coatings as well, since the nitroanisole core enables light-absorption and tuning mechanical properties through later-stage substitutions.

    Why Source Directly from the Manufacturer?

    Talking directly with buyers and R&D teams, we hear plenty of stories about mixed-batch lots, unlabeled process residues, and shipping delays from third-party resellers. There’s a noticeable difference working with a team where everyone—chemists, logistics, QA—operates under the same roof and agrees on standards. We control every input and output, keep full traceability, and quickly answer questions about synthesis dates, origin of starting materials, or batch-specific variability.

    A direct manufacturing approach means we can accommodate custom requests, too. Some clients ask for additional purification, custom-sized containers, or modified drying protocols for regulatory reasons. Because we oversee the plant floor, not just a warehouse, our team can pivot quickly, ensuring the product suits actual usage—not just a catalog listing. Having learned from years of fielding last-minute regulatory changes and formulation needs, we keep a flexible posture, but with the solid backbone of batch-to-batch consistency.

    Another important aspect relates to environmental stewardship. Chemical manufacturing leaves a footprint, so we have spent time and funds refining waste handling and solvent recycling. Our plant runs on closed-loop systems for halogen recoveries, and our analytical team updates waste tracking in real time. Investing directly in these improvements means our products meet both technical and ethical standards expected by modern industry partners and regulators.

    Product Differences: Knowledge Earned from Hard Work

    It’s easy to lump nitroanisole derivatives together, but real-world applications expose the clear differences. Over the years, we’ve tested competitor lots of 4-Bromo-2-Fluoro-6-Nitroanisole alongside our own batches. Some came laden with unreacted parent anisole or brimming with mixed halogen isomers, delivering unpredictable reactivity. The difference isn’t just analytical—it shows up during the first step of a catalytic reaction or the first crystallization of an API intermediate. Our rigorous in-line controls, paired with months of pilot-scale process optimization, give chemists materials that react as the literature predicts.

    A handful of our customers once relied on a structurally similar compound: 2-Fluoro-6-Nitroanisole. In practice, that material struggles with subsequent cross-coupling and provides lower yield, especially for sensitive nucleophilic substitutions. The extra reactivity from the para-bromine in our product brings new options to retrosynthetic planners. Teams working on manufacturing scale-ups tell us that non-uniform particle size or excess moisture throws off downstream processes. We invested heavily in drying and sieving equipment, and the uniformity we now achieve comes not from luck but from patient trial-and-error guided by seasoned floor operators.

    Down-to-Earth Guidance for New Users

    Not every chemist knows what to expect the first time they use a specialty halogenated nitroanisole. After seeing dozens of successful and failed runs, our own technical support staff can walk users through common pitfalls. For instance, moisture content throws off certain reactions—so pre-drying, even in a well-sealed container, matters. Subtle batch-to-batch differences in crystalline habit may impact bulk handling, especially in automated feeders. The advice we give: store cool and dry, open only as needed, and don’t mix partial lots unless all are from the same batch and purity profile.

    We’ve walked customers through more than one last-minute triage, talking through everything from GC troubleshooting to solubility tweaks. On the rare occasion things do go sideways, we’ve always prioritized hands-on help, not finger-pointing. Customers deserve straight talk and, when required, expedited replacement material or a frank discussion on failed process steps. Our reputation is only as good as the product’s actual performance, so we never shy away from feedback—good or bad.

    The Future: Delivering Reliability

    Every sector we serve, from pharmaceutical research to advanced materials, expects tighter specifications and faster response than ever before. Years back, a five-day shipping window seemed fine, but now rapid turnaround is standard, and clients expect certificates of analysis with exhaustive detail. We’ve adapted by expanding both technical staff and front-line customer support, anticipating not just the next query about grade or container type but the deeper questions about sustainability, traceability, and regulatory status.

    We regularly update our processes, add new testing equipment, and train every new team member on both the chemistry and the “why” behind our protocols. We listen to feedback from the bench, the plant floor, and the regulatory desk, using real-world lessons to guide our improvements. Batch-to-batch reliability, clear communication, and a true partnership approach set us apart from generic commodity traders. Our track record supplying 4-Bromo-2-Fluoro-6-Nitroanisole to industry leaders, university labs, and innovative startups proves that a manufacturer’s knowledge isn’t just technical—it’s practical, learned, and always evolving.

    Final Thoughts from the Manufacturer’s Side

    Every order that leaves our facility represents hundreds of small choices—raw material supplier selection, analytical method validation, reactor cleaning, segregated storage, and the experienced eyes of our plant staff who’ve spotted things that machines and software still miss. We keep a close-knit culture on the shop floor, trusting that open conversations, shared responsibility, and direct accountability yield better results than top-down mandates or outsourced control.

    4-Bromo-2-Fluoro-6-Nitroanisole stands as more than just a compound in a container. It reflects years of trial, feedback, and adjustment made by real people working side by side. We will keep doing whatever it takes to ensure our product supports breakthroughs in research, process chemistry, and real-world applications. From our team to yours, reliability is not a slogan—we stake our reputation on it, and we work every day to keep earning that trust.