2-Bomo-5-fluoropyridine

    • Product Name: 2-Bomo-5-fluoropyridine
    • Chemical Name (IUPAC): 2-bromo-5-fluoropyridine
    • CAS No.: 65610-40-8
    • Chemical Formula: C5H3BrFN
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    173981

    Chemicalname 2-Bromo-5-fluoropyridine
    Casnumber 79456-24-1
    Molecularformula C5H3BrFN
    Molecularweight 175.99
    Appearance Colorless to pale yellow liquid
    Boilingpoint 192-194°C
    Density 1.69 g/cm³
    Purity Typically ≥98%
    Solubility Soluble in organic solvents (e.g. DMSO, methanol)

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

    Packing & Storage
    Packing 2-Bromo-5-fluoropyridine is supplied in a 25g amber glass bottle with a tamper-evident cap and hazard labeling.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 2-Bromo-5-fluoropyridine: Securely packed in drums or bottles, palletized, moisture-protected, optimal space utilization, compliant with transport regulations.
    Shipping 2-Bromo-5-fluoropyridine is shipped in tightly sealed containers, protected from moisture and light, and labeled according to hazardous material regulations. It is transported as a chemical substance—potentially classified as hazardous—requiring adherence to international, national, and local shipping guidelines for flammable, toxic, or environmentally hazardous chemicals.
    Storage 2-Bromo-5-fluoropyridine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. The storage area should be equipped to contain spills and labeled clearly. Personal protective equipment should be used when handling this chemical to prevent skin and eye contact.
    Shelf Life 2-Bromo-5-fluoropyridine has a shelf life of 2 years when stored in a cool, dry, and tightly sealed container.
    Application of 2-Bomo-5-fluoropyridine

    Purity 99%: 2-Bomo-5-fluoropyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurity formation.

    Melting Point 40-44°C: 2-Bomo-5-fluoropyridine with a melting point of 40-44°C is used in fine chemical manufacturing, where controlled solidification improves separation efficiency.

    Molecular Weight 176.96 g/mol: 2-Bomo-5-fluoropyridine of molecular weight 176.96 g/mol is used in heterocyclic compound development, where precise stoichiometry supports consistent reaction outcomes.

    Stability Temperature up to 60°C: 2-Bomo-5-fluoropyridine with stability temperature up to 60°C is used in agrochemical synthesis, where thermal robustness maintains chemical integrity.

    Low Moisture Content <0.5%: 2-Bomo-5-fluoropyridine with low moisture content <0.5% is used in organofluorine material preparation, where reduced hydrolysis risk enhances product stability.

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    Certification & Compliance
    More Introduction

    2-Bromo-5-fluoropyridine: A Modern Take on Pyridine Derivatives

    A Closer Look at 2-Bromo-5-fluoropyridine

    Every day in a research environment brings fresh challenges, especially when the project calls for building custom molecules or tuning complex reactions. Over the years, scientists and process chemists have explored a host of building blocks, looking for versatility, efficiency, and reliability. Pyridines always stand out because of their adaptability in organic synthesis. Among the many options, 2-Bromo-5-fluoropyridine carries its own weight as a distinct model—both for its reactivity and for the way it shapes chemical development.

    This pyridine derivative has gained ground in both medicinal chemistry and materials science, due to the specific placing of its bromo and fluoro groups on the pyridine ring. Structurally, it’s simple: a bromine atom at the second position and a fluorine at the fifth, nestled onto the classic six-membered nitrogen-containing ring. In practice, this layout marks a critical difference from other substituted pyridines that may have halogens placed elsewhere, or only one halogen at all.

    Why Chemists Value 2-Bromo-5-fluoropyridine

    Chemists in the lab know that sometimes a single functional group makes or breaks a project. Here, the bromo atom ups the ante by offering a highly reactive site ready for classic coupling reactions—think Suzuki or Buchwald-Hartwig coupling. It’s the kind of handle you look for when you want to stitch two fragments together with precision. The fluorine brings its own set of perks. Not only does it offer metabolic stability in bioactive compounds, but it also tweaks the electronic character of the ring, shifting reactivity in subtle ways. Pairing bromine and fluorine gives scientists a handle on both reactivity and downstream molecular function, creating new possibilities in lead optimization or agrochemical development.

    Anyone who’s sat through a string of failed reactions knows the headaches of unstable or overly bulky reagents. 2-Bromo-5-fluoropyridine remains more than manageable at the bench. Its relatively low molecular weight keeps it mobile as a crystallized solid, easy to weigh, transfer, and dissolve, whether you’re scaling up for a kilo-lab or doing a microgram-scale library expansion. In my own research, switching from a bulkier halogenated pyridine to 2-Bromo-5-fluoropyridine meant faster purification and fewer side products, especially during cross-coupling runs.

    Comparing It to Other Pyridine Building Blocks

    It’s tempting to lump all halogenated pyridines together. But differences in the halogen’s position or type quickly show themselves once the reactions start. For instance, swapping bromine for chlorine might sound minor, but bromine is far more amenable to oxidative addition, a crucial step in many transition-metal catalyzed processes. Even two bromines on the same ring produce different patterns of reactivity compared to this bromo-fluoro mix. Fluorine at the fifth spot helps fine-tune electron density, nudging the molecule toward specific outcomes in coupling, nucleophilic aromatic substitution, or further functionalization.

    Over time, chemists and chemical engineers noticed that compounds like 3-bromo or 4-fluoropyridine didn’t match the performance of 2-Bromo-5-fluoropyridine in certain pharmaceutical intermediates or material precursors. The difference isn’t academic: selecting the right isomer slashes side reactions and can boost target yields, which pays off not just in saved time but in reduced material costs and waste.

    Key Applications in the Real World

    The most common use for 2-Bromo-5-fluoropyridine remains as a starting point in the synthesis of advanced pharmaceutical candidates. Medicinal chemists have gravitated toward it for introducing rigid, metabolically stable motifs in kinase inhibitors and CNS drugs. Adding to this list, crop protection scientists have leveraged the bromo-fluoro skeleton for designing fungicides and herbicides with targeted spectra.

    Beyond small molecules, material scientists have taken note of its electron-withdrawing profile. It fits into polymers, dyes, and specialty electronics, especially where controlled electron flow matters. Here, the fluorine tailors physical properties, while the bromo is tailored in for post-polymerization modification. In electronic materials, properties like dielectric strength and chemical durability start with such design elements, and well-chosen building blocks make a marked difference.

    Unique Model and Specifications

    2-Bromo-5-fluoropyridine typically appears as an off-white to pale yellow crystalline solid or powder, stable under dry, ambient storage. Molecular formula: C5H3BrFN. Molecular weight hovers near 175 grams per mole, a sweet spot for both reactivity and ease-of-use in reaction planning.

    Boiling points, solubility, and melting characteristics make prep work and isolation less troublesome. Solubility in polar aprotic solvents is usually strong—DMSO, DMF, and acetonitrile remain chemists’ favorites for smooth reactions. From a work-up perspective, flash chromatography or crystallization are the usual methods, without the quirks of some less stable pyridine analogues.

    Focusing on Safety and Handling

    There’s a reason good research teams stress safety and compliance, beyond just avoiding regulatory headaches. Commercial 2-Bromo-5-fluoropyridine normally carries hazard designations because of the presence of both bromine and fluorine—both add reactivity, and the pyridine ring itself can cause irritation if handled carelessly. Lab handling calls for adequate ventilation and solid personal protective gear. This isn’t just formality: I’ve seen projects stumble when labs skipped out on standard gloves or ventilation, setting back timelines for days or even weeks.

    Waste management matters here as well. Disposal follows established protocols for halogenated aromatic organics, preferably by professionals with the right destruction facilities. Even in small quantities, waste can stack up quickly as process development scales, so planning ahead pays off.

    Current Trends and Industry Demand

    An uptick in demand for 2-Bromo-5-fluoropyridine tracks with the broader shift toward precision in medicinal chemistry. Drug makers and research organizations demand building blocks with exacting consistency, laid-out purity profiles, and reliable supply chains. As a result, the marketplace began to host more high-purity grades, sometimes audited with full spectroscopic analysis—NMR, GC-MS, and HPLC—all aimed at making sure nothing unwanted slips into critical syntheses.

    Modern bioactive compound design often hinges on late-stage functionalization, and intermediates like 2-Bromo-5-fluoropyridine provide a launching pad for these techniques. I’ve worked with medicinal chemists who build dozens of analogues in a week—using this compound as the central pivot to introduce new side chains, heterocycles, or linkers that tailor pharmacological profiles down to the smallest detail.

    Challenges Associated with 2-Bromo-5-fluoropyridine

    Working with 2-Bromo-5-fluoropyridine is generally straightforward, but issues do crop up. Sometimes buyers run into supply volatility—due either to inconsistent global raw material streams or production shutdowns. Halogenated building blocks are subject to swings in bromine prices, and strict environmental oversight adds layers to sourcing and transportation.

    Scaling up is another common issue: What works smoothly at bench scale can run up against heat transfer, mixing, or solvent safety concerns at 100-gram or kilogram scale. Reaction exotherms, sometimes mild in flasks, can surprise a pilot plant. Quality control tightens too: re-crystallization, distillation, and handling protocols get stricter as batch sizes grow, especially to satisfy regulatory filings or quality audits by pharmaceutical partners.

    Potential Solutions and Best Practices

    From years navigating chemical supply, a few practices stand out. Reliable sourcing starts with trusted suppliers—ones that back up quality with thorough lab analysis and clear batch documentation. Open communication keeps surprises at bay, whether by asking up front for batch data, impurity thresholds, or even a stability report.

    Scaling up also calls for a staged approach: pilot small, then grow in stepwise fashion. More than once, I’ve seen problems caught early by running intermediate-batch syntheses under scaled-up conditions. This approach shortens timelines, prevents rework, and often cuts unnecessary costs. Well-trained technicians and good documentation smooth the transition, keeping teams focused and safe as production ramps.

    On the regulatory and environmental side, companies and labs that invest early in responsible waste treatment avoid later pressures. Modern facilities opt for localized halogen handling and solvent recovery, both safer for personnel and more cost-effective over time. These investments also win goodwill with environmental agencies—a factor not to underestimate in today’s research landscape.

    Shaping Innovation Through Careful Selection

    Choosing 2-Bromo-5-fluoropyridine over another substituted pyridine isn’t a matter of routine—it’s about asking what your project needs and what trade-offs you’re willing to make. Substituents matter at every stage: the right choice can add months of patent life or cut a difficult process step. There’s a confidence that comes from relying on a compound whose behavior matches expectations, especially in projects where timelines are tight and budgets don’t stretch far.

    I’ve seen the real savings—not just in cash but in decreased complexity—by building synthetic plans focused on reliable intermediates. In team settings, experienced chemists swap stories of agonizing troubleshooting with troublesome reagents, and winning formulas always feature proven, well-characterized building blocks. Over the years, 2-Bromo-5-fluoropyridine has carved out trust among process chemists and researchers because of this kind of dependability.

    The Path Forward for 2-Bromo-5-fluoropyridine

    Industry interest in fluorinated and brominated pyridines keeps building as research into novel drugs and specialty materials quickens. Whether in pharma, crop protection, or functional polymers, labs favor intermediates with robust documentation, consistent availability, and versatile chemistry. The trend toward high-purity, well-characterized tools won’t let up—especially as patent windows shrink and competition intensifies.

    Respecting reproducibility and transparency has become more than good form; it’s now an expectation. Research managers push for traceability, and clients ask pointed questions about source, byproducts, and environmental impact. 2-Bromo-5-fluoropyridine keeps fitting into this evolving landscape, not just as a tool but as a model for future building blocks—meeting rising quality standards while continuing to deliver flexibility in design.

    Encouraging Further Exploration

    Innovation doesn’t arise from routine. Trying new combinations or variations often starts with one reliable component. What 2-Bromo-5-fluoropyridine offers is a familiar yet remarkably flexible cornerstone—one that both early-career and seasoned chemists can learn from and build upon. Bringing fresh eyes to known compounds often results in creative applications, new routes, or entirely different outcomes that change understanding altogether.

    Continued investment in process improvement means both refining production and supporting end-users in the lab with better data, packaging, and support services. Forward-looking labs see this not just as a necessity but as a path to collaboration—one that ensures the whole R&D ecosystem benefits, from the synthetic bench all the way to end products that improve health, safety, or functionality.

    Conclusion: A Quiet Keystone in Modern Synthesis

    2-Bromo-5-fluoropyridine stands as more than just another tool on the shelf. Its unique mix of reactivity and adaptability has made it a staple for those shaping new medicines, fine chemicals, and functional materials. Everyone from discovery researchers to process scale-up teams trusts it not just for what it can do alone, but for the doors it opens across chemistry’s broad landscape. In a fast-moving field, tools that offer both dependability and innovation keep science moving forward, one carefully chosen building block at a time.