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5-Bromo-2-Fluoro-3-Methoxypyridine

    • Product Name 5-Bromo-2-Fluoro-3-Methoxypyridine
    • Alias 5-Bromo-2-fluoro-3-methoxy-pyridine
    • Einecs 821-477-5
    • 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
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    Specifications

    HS Code

    956435

    Productname 5-Bromo-2-Fluoro-3-Methoxypyridine
    Casnumber 886373-36-6
    Molecularformula C6H5BrFNO
    Molecularweight 206.02
    Appearance White to off-white solid
    Meltingpoint 47-50 °C
    Purity ≥98%
    Solubility Soluble in organic solvents
    Smiles COC1=C(C=NC(=C1)F)Br
    Inchi InChI=1S/C6H5BrFNO/c1-10-6-4(7)2-3-9-5(6)8
    Storageconditions Store at room temperature, dry and sealed

    As an accredited 5-Bromo-2-Fluoro-3-Methoxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 5-Bromo-2-Fluoro-3-Methoxypyridine

    Applications of 5-Bromo-2-Fluoro-3-Methoxypyridine in Industrial Manufacturing

    As a direct manufacturer, we supply 5-Bromo-2-Fluoro-3-Methoxypyridine for strictly defined industrial sectors where its structural features provide specific performance advantages. Below, we outline primary downstream manufacturing environments where this intermediate proves essential, detailing compliance, usage, process integration, and end product examples within each scenario.

    1. Pharmaceutical Intermediate Synthesis for Oncology APIs

    5-Bromo-2-Fluoro-3-Methoxypyridine plays a critical role as a building block in oncology-focused active pharmaceutical ingredient (API) routes, especially for pyridine-containing heterocyclic scaffolds used in kinase inhibitors. Pharmaceutical manufacturers incorporate this raw material at specific synthetic junctures for targeted functionalization, ensuring purity and reactivity consistent with stringent medicinal product requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • European Pharmacopoeia (Ph. Eur.) monographs (where finished API is registered)
    • China Pharmacopoeia (for local registrations)

    Typical usage ratio

    • 0.8–1.2 molar equivalent per target core fragment; slight excess selected based on specific downstream route optimization and impurity control strategy

    Downstream process integration

    • Added after initial pyridine ring framework construction, prior to halogen exchange or etherification steps, and typically followed by Suzuki or Buchwald–Hartwig coupling in multi-step API synthesis

    Final product types

    • Small molecule kinase inhibitor APIs for parenteral or oral oncology therapeutics
    • Specialty intermediates further processed for targeted pharmaceutical agents

    2. Agrochemical Intermediate Manufacturing for Herbicides

    Major agrochemical industry participants utilize this material for synthesizing pyridine-based herbicide actives, particularly in compounds requiring brominated and fluorinated pyridine motifs for enhanced biological activity. It enters the synthesis stream where functionalized heterocycles are required as key intermediates for crop protection agents with defined residual profiles.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • OECD Principles of Good Laboratory Practice (GLP) for tech-grade material qualification
    • Chinese GB/T 1604 for pesticide intermediate quality

    Typical usage ratio

    • 5–10% by mass relative to batch scale of the primary herbicide intermediate; formula varies based on the catalytic conversion yield and downstream halogenation routes

    Downstream process integration

    • Introduced after Grignard or amination steps; typically forms part of the coupling reaction to generate highly substituted pyridine cores in herbicidal molecules

    Final product types

    • Post-emergence selective herbicides containing pyridine derivatives
    • Pre-emergent soil-acting weed control agents

    3. Manufacture of Advanced Electronic and Display Materials

    Electronic chemical formulators use this intermediate for specialty molecular design projects, particularly for constructing pyridine-based ligands and charge transport materials suited to organic light-emitting diode (OLED) devices and thin-film transistors. Fine electronic manufacturers specify this grade when synthesizing custom heterocyclic compounds with demanding electrical and photophysical property requirements.

    Industry compliance standards

    • Electronic chemicals must comply with SEMI C3 purity standards (for organic electronic materials)
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU)
    • RoHS Directive 2011/65/EU restrictions (for final devices)

    Typical usage ratio

    • 3–7% by mass in precursor mixtures for small-molecule OLED material batches; adjusted per synthetic yield and required end-use volatilization performance

    Downstream process integration

    • Incorporated post-ligand synthesis during coupling procedures, either via Suzuki-type or Stille reactions, prior to purification for device-grade organic molecules

    Final product types

    • OLED emitter/host materials
    • Printable organic semiconductors for flexible displays

    4. Specialty Chemical Synthesis for Medical Imaging Contrast Agents

    Leading developers of medical imaging products employ this raw material to assemble precursor structures involved in the synthesis of radiolabeled pyridine-based contrast agents. The methoxy, bromo, and fluoro substitution pattern is essential for achieving optimal in vivo performance, dictating the selectivity and hydrophilicity of imaging probes for both PET and SPECT modalities.

    Industry compliance standards

    • US Pharmacopeia (USP) general chapters for imaging agents
    • cGMP standards for Active Pharmaceutical Ingredients (21 CFR Part 210/211)
    • ISO 13485 for quality management in medical device production

    Typical usage ratio

    • 0.5–1.3 molar equivalent per radiolabel precursor batch, adjusted for radiochemical conversion efficiency and specific isotope incorporation chemistry

    Downstream process integration

    • Used in late-stage precursor arylation and functionalization before radiolabel introduction, often via nucleophilic substitution or palladium-catalyzed coupling

    Final product types

    • Positron emission tomography (PET) contrast agents
    • SPECT imaging probes incorporating functionalized pyridine ligands

    5. Intermediate for Veterinary Drug Development

    Veterinary API manufacturers source this pyridine intermediate for synthesis routes involving anti-parasitic and anti-inflammatory agents commonly used in livestock and companion animal care. Its specific halogenated and methoxylated structure accommodates advanced lead modification strategies in veterinary drug research and production pipelines.

    Industry compliance standards

    • VICH GL guidelines for veterinary pharmaceutical development
    • US FDA Center for Veterinary Medicine (CVM) regulations
    • European Pharmacopoeia veterinary monographs (where applicable)

    Typical usage ratio

    • 0.7–1.1 molar equivalent, determined by the complexity of the target structure and the required activity spectrum of the final drug candidate

    Downstream process integration

    • Functions as a coupling component in the core build of the active moiety, used before protective group removal and salt formation in final API crystallization

    Final product types

    • Veterinary oral or injectable anti-parasitic drugs
    • Livestock-targeted anti-inflammatory medications
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    More Introduction

    5-Bromo-2-Fluoro-3-Methoxypyridine: A Key Building Block for Modern Chemistry

    Working in a chemistry lab opens your eyes to the building blocks that drive pharmaceutical research and new materials. Among these, 5-Bromo-2-Fluoro-3-Methoxypyridine often comes up when projects demand something beyond what the typical pyridine derivatives can offer. In chemical research, a single atom swap can do more than just change a molecule’s look—it changes the entire course of a synthesis and the performance of the end product.

    The model number for this compound—CAS 261953-36-6—serves as a useful marker for researchers hunting through chemical catalogs. The molecular make-up offers more than just a scaffold; it brings together the potent influence of a bromine atom, the selectivity of a fluorine, and the versatility of a methoxy group. Often, those who have worked with other pyridine compounds notice that the combination present in 5-Bromo-2-Fluoro-3-Methoxypyridine opens doors that either compound class alone could not. The molecular formula C6H5BrFNO summarizes its composition, but the significance comes out in lab tests.

    What Sets This Compound Apart

    Some might wonder what the fuss is with small changes like adding a bromine or a fluorine. In years of experience with organic synthesis, plenty of projects have ground to a halt because a molecule just wouldn’t react as needed. Incorporating fluorine tends to strengthen carbon-fluorine bonds and often helps drugs better survive metabolism. The methoxy group, on the other hand, brings greater solubility and flexibility—it helps dissolve molecules in both research solvents and biological media. Attaching a bromine opens the door for further cross-coupling reactions using well-known techniques like Suzuki or Buchwald-Hartwig.

    The specific substitutions on this pyridine core aren’t just for show. Each functional group works together, making this molecule fit for complex projects. Many researchers in pharmaceutical labs choose this compound as a starting point when seeking structure-activity relationships because these modifications let them fine-tune both chemical properties and biological responses. With thousands of variations out there, pyridines remain a mainstay, but in my own work, this one often appears in experimental plans when broader reactivity or increased stability becomes crucial.

    Applications and Practical Use

    Medicinal chemistry often deals with challenges that come from unstable intermediates or tricky reaction conditions. Having worked with large teams focused on improving lead compounds for new drugs, I’ve noticed 5-Bromo-2-Fluoro-3-Methoxypyridine emerges as a favorite choice during the optimization step. Its reactivity profile stands out in carbon-carbon bond formation, halogen exchange, and expansion into triazine and pyrimidine scaffolds. Colleagues have frequently turned to this compound when standard halopyridines failed to give the desired product without degradation.

    Beyond pharmaceuticals, this molecule finds use in crop protection research, where unique pyridine derivatives enable better efficacy and lower application rates. Following reports from agricultural chemistry journals, products derived from halogenated methoxypyridines sometimes outperform older chemistries by disrupting resistance in field pests. In a practical sense, I’ve observed projects cut months from their timelines by adapting routes that include this intermediate, sidestepping the purification headaches that tangle up rival compounds.

    Material science groups also find value in molecules like 5-Bromo-2-Fluoro-3-Methoxypyridine. Developing functionalized polymers, flame retardants, or custom catalysts often requires heterocyclic building blocks that withstand tough processing conditions. The specific arrangement found here offers a balance—reactive enough to build on, stable enough to survive scaling up. Industry reports echo what many in the lab learn first-hand: a single smart substitution makes downstream chemistry less risky.

    Specifications and Handling

    Lab work always brings safety concerns, especially when working with halogenated organics. This compound typically presents as a colorless or pale yellow solid, requiring standard precautions familiar to anyone who handles similar pyridine rings. Weighing, dissolving, and reacting often go smoothly compared to more volatile analogs. Laboratories often note its melting point in the 40-50°C range and its reasonable solubility in common organic solvents such as dichloromethane, acetonitrile, and THF.

    The purity expectation for modern research—often quoted at over 98%—reflects the demands of high-stakes pharmaceutical development. Most reputable suppliers use rigorous chromatography and constant batch analysis to keep impurities at bay. Elevated purity saves time since researchers avoid repeating failed reactions or wrestling with ambiguous NMR spectra. Several times in my own lab experience, impurities in similar compounds have caused needless troubleshooting that set projects back, so I respect the strict bar set for this kind of reagent.

    How It Stands Out From Similar Products

    On paper, plenty of pyridine derivatives offer a blend of halogen and methoxy groups, but most combine substitutions in a pattern that doesn’t lend itself to modern synthetic techniques. Step into any medicinal chemistry meeting and mention 5-Bromo-2-Fluoro-3-Methoxypyridine—seasoned scientists recognize it for the finely tuned balance among reactivity, metabolic resilience, and synthetic accessibility.

    In actual practice, switching out bromine for chlorine on the same ring changes both the cost structure and the range of reactions. Chlorinated pyridines tend to resist cross-coupling, which often leads chemists to abandon them mid-project. The presence of fluorine, in contrast, can also serve as a unique marker in biological studies that use NMR, making this specific derivative resourceful both in discovery and analysis. Comparing it with pyridines missing the methoxy group highlights a marked drop in solubility, which causes delays during the purification stage or when scaling up.

    From personal experience, I’ve seen teams wrestle with analogs that seemed promising but ultimately failed due to small changes—a missing methoxy or swapped halogen. The trouble usually appears too late, often after invest hours or weeks into syntheses. With 5-Bromo-2-Fluoro-3-Methoxypyridine, difficulty seldom comes down to the compound’s failings. Issues, if any, arise from ambitious project goals, not from instability or uncooperative reactivity.

    Standing Up to Quality Demands

    Clients and regulators expect complete data before any synthesized product leaves the lab. This stretches from NMR spectra to LC-MS readings and elemental analysis. Over the years, I’ve seen the list of required documentation grow as the stakes in pharmaceutical and agricultural research went up. This compound’s popularity among accredited labs does not surprise me one bit—its stability and reliable spectra create fewer red flags, smoothing audits and approval cycles.

    Researchers also place value on traceability. Whenever a project faces regulatory review, clear batch records and proven synthesis routes matter. Manufacturers that offer this compound at scale know the importance of batch-to-batch reproducibility, which comes into play during long-term studies or when product recalls loom in other industries. Consistency in handling and identity testing matters, and I’ve seen labs choose lower-yielding but more consistent sources after running into mystery impurities from less careful suppliers.

    Supporting Evidence and Scientific Value

    Literature reviews and patent filings show this compound’s frequent appearance in the early stages of drug development pipelines. In journals like the Journal of Medicinal Chemistry, examples pop up where a swap between fluorine and hydrogen on a pyridine ring produced big jumps in binding affinity or selectivity for target enzymes. Synthetic methods using the bromo position often open routes that aid medicinal chemists in exploring new pharmacophores, which means more options when lead compounds fail to deliver in animal studies.

    Analytical chemistry teams value the fluorinated position for its clear signals in NMR, a detail that aids purity assessment and tracking metabolites. The methoxy group, meanwhile, improves handles for further chemistry and can help increase bioavailability in many animal models. My own projects have benefited from these features, particularly in last-minute troubleshooting, where switching to this compound kept synthesis cycles on track.

    Agricultural and materials research also leverage pyridine’s modular nature. Surveys of crop protection patents reveal the use of specialized pyridines to develop not just new herbicides and fungicides, but also adjuvants that improve application. Polymer scientists sometimes use halogenated pyridines as chain extenders or to introduce new physical properties—this often adds durability or fire resistance, which in turn leads to safer products on the market.

    Toward More Responsible Chemistry

    Environmental and safety considerations keep growing in importance. Organic chemists today face regulatory pressure to minimize hazardous waste and avoid persistent pollutants. Products like 5-Bromo-2-Fluoro-3-Methoxypyridine, with their higher efficiency and targeted reactivity, reduce byproducts and simplify purification, which means less solvent usage and waste disposal. This isn’t just a minor benefit; teams working under tight green chemistry guidelines rely on every small edge.

    From a broader perspective, using more stable building blocks like this one can cut down on project delays from contamination or failed purification. In several industrial projects I worked on, stricter environmental guidelines forced teams to abandon tricky intermediates that gave off noxious byproducts. By swapping in better-behaved molecules, we finished ahead of schedule and passed both internal and external audits, which saved both money and reputation.

    The shift toward renewable and sustainable synthesis sometimes involves more than just swapping feedstocks. Molecules like 5-Bromo-2-Fluoro-3-Methoxypyridine support safer, more efficient research by slashing avoidable bottlenecks in downstream processing. This sort of chemical progress supports regulatory, commercial, and scientific goals—all while keeping operations cleaner and safer for workers.

    Solutions for Common Challenges

    Even popular intermediates present their share of lab troubles. Over the years, several recurring issues have come up: scaling reactions without loss of purity, ensuring complete reactions in cross-coupling, and troubleshooting unexpected byproducts. The common fixes rest on careful reaction optimization and clear communication with suppliers. Using fresh, high-purity 5-Bromo-2-Fluoro-3-Methoxypyridine cuts down on headaches and ambiguous results.

    For labs working at scale, choosing a supplier with strong logistics and traceable documentation makes a difference. Having seen projects stumble due to undisclosed impurities, my team began to rely on established production partners who ran extra HPLC and GC-mass checks. Faster access to analytical data gives project leads the confidence to move forward without costly re-dos. This compound, in my own experience, frequently arrives in ready-to-go packaging that holds up during long storage, reducing error at the bench.

    Reaction optimization starts at the planning stage. Some projects find themselves running up against sluggish coupling reactions. Small adjustments—selecting the right ligand or changing solvent—can turn a frustrating dead-end into a productive route. Having a reliable intermediate with defined reactivity makes trial-and-error less fraught, trading guesswork for real progress. Working with this molecule over several product cycles has shown me the value of predictability—every setback avoided shaves weeks off development.

    Community Impact and Ongoing Development

    Teaching new chemists about synthesis means helping them see the difference between theoretical pathways and those that work in the lab. I’ve used compounds like 5-Bromo-2-Fluoro-3-Methoxypyridine as real-life examples. Because it articulates so well with modern methods and highlights the benefits that come from even small functional group tweaks, it gives students a practical window into structure-activity relationships.

    As research shifts from trial-and-error to more data-driven methods, the need for well-characterized intermediates like this one keeps growing. People want to know the chemistry works, the data holds up, and the environmental footprint stays manageable. Consistent results free up time to focus on more challenging aspects—whether that’s computational modeling, rapid prototyping, or advanced biological testing.

    There’s a sense of collective progress in using high-quality materials. Drug developers, farmers, engineers—all depend on reliable chemical inputs. Reports from the field confirm that the unique properties of this molecule provide measurable performance boosts in projects that range from health to materials to food security. Collaboration between chemists and end-users fuels innovation and addresses both technical and social needs, raising the bar for what chemistry can offer society.

    Looking Forward

    With research budgets stretched and regulatory oversight increasing, laboratories need building blocks they can trust to perform as advertised. My own journey in applied chemistry continues to highlight the advantages of intermediates that work without drama—those that do what you expect, day after day. 5-Bromo-2-Fluoro-3-Methoxypyridine demonstrates that carefully-chosen substitutions and consistent production standards can reshape research timelines, boost product quality, and support safer, more responsible science.

    As researchers face new pressures—from global competition to rising safety standards—the compounds they choose become more than just ingredients. They represent a commitment to accuracy, progress, and shared benefit. 5-Bromo-2-Fluoro-3-Methoxypyridine stands out by supporting these goals, marking an important step forward in the way chemical sciences move from concept to impact.