3-Bromo-2-fluoropyridine

    • Product Name: 3-Bromo-2-fluoropyridine
    • Chemical Name (IUPAC): 3-Bromo-2-fluoropyridine
    • CAS No.: CAS 57381-51-6
    • Chemical Formula: C5H3BrFN
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    896457

    Cas Number 871329-44-7
    Molecular Formula C5H3BrFN
    Molecular Weight 191.99
    Appearance Colorless to pale yellow liquid
    Purity ≥98%
    Boiling Point 189-191°C
    Density 1.69 g/mL at 25°C
    Refractive Index 1.566
    Flash Point 70°C
    Smiles C1=CC(=NC=C1Br)F
    Solubility Slightly soluble in water, soluble in organic solvents
    Storage Temperature 2-8°C
    Synonyms 3-Bromo-2-fluoro-pyridine

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3-Bromo-2-fluoropyridine, sealed with a screw cap and labeled with hazard information.
    Container Loading (20′ FCL) Container loading (20′ FCL) for 3-Bromo-2-fluoropyridine ensures secure, moisture-free bulk chemical transport in sealed 200 kg HDPE drums.
    Shipping 3-Bromo-2-fluoropyridine is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is transported in compliance with relevant hazardous material regulations, typically by ground or air, and kept away from sources of ignition, moisture, and incompatible substances. Proper labeling and documentation accompany each shipment to ensure safety and traceability.
    Storage 3-Bromo-2-fluoropyridine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. The storage area should be clearly labeled and equipped for handling volatile organic compounds, with appropriate chemical spill containment measures in place to prevent exposure and environmental contamination.
    Shelf Life 3-Bromo-2-fluoropyridine typically has a shelf life of 2-3 years when stored in a cool, dry, and tightly sealed container.
    Application of 3-Bromo-2-fluoropyridine

    Purity 98%: 3-Bromo-2-fluoropyridine with 98% purity is used in pharmaceutical intermediate syntheses, where it ensures high-yield coupling reactions.

    Molecular weight 176.98 g/mol: 3-Bromo-2-fluoropyridine with a molecular weight of 176.98 g/mol is used in agrochemical research, where its defined mass allows precise formulation adjustments.

    Melting point 10-12°C: 3-Bromo-2-fluoropyridine with a melting point of 10-12°C is used in organic electronics manufacturing, where its low melting range facilitates solution processing.

    Boiling point 191-193°C: 3-Bromo-2-fluoropyridine with a boiling point of 191-193°C is used in fine chemical synthesis, where its volatility supports controlled distillation.

    Stability temperature up to 60°C: 3-Bromo-2-fluoropyridine stable up to 60°C is used in storage of chemical libraries, where its thermal resilience maintains compound integrity.

    Low water content <0.2%: 3-Bromo-2-fluoropyridine with water content below 0.2% is used in anhydrous reactions, where minimal moisture prevents side reactions.

    Particle size <50 μm: 3-Bromo-2-fluoropyridine with particle size less than 50 μm is used in formulation of solid reagents, where fine particles enhance dissolution rates.

    GC assay ≥99%: 3-Bromo-2-fluoropyridine with GC assay not less than 99% is used in high-purity synthesis, where analytical assurance ensures reproducibility of results.

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    Certification & Compliance
    More Introduction

    3-Bromo-2-fluoropyridine: A Versatile Building Block for Innovation

    Discovering Value in 3-Bromo-2-fluoropyridine

    Chemistry often comes down to the building blocks people choose. Some molecules just seem to make things click together a little more smoothly, and 3-Bromo-2-fluoropyridine is one of those. With a molecular formula of C5H3BrFN, this compound takes the solid, reliable backbone of pyridine and tweaks it with both a bromine and a fluorine group. The result is a molecule that does more than you'd expect from its small size.

    Having worked in laboratory settings and followed the growth of pharmaceutical and specialty chemical development, I have watched this compound pop up with surprising regularity in both research and industrial settings. That says a lot about its flexibility and power as a starting material. The reason behind it comes down to chemistry: the bromo and fluorine groups sitting at different positions on the pyridine ring give researchers more control over chemical transformations. You're not locked into one path; there's room to maneuver and create what’s needed.

    Molecular Details and Practical Implications

    3-Bromo-2-fluoropyridine’s structure gives synthetic chemists a unique combination—extending both reactivity and selective transformation possibilities. The presence of bromine at the third position often brings in cross-coupling opportunities, like Suzuki, Sonogashira, and Buchwald-Hartwig reactions. Fluorine throws in its own effects—electronegativity and bond strength, shifting the reactivity of the other positions on the ring.

    People talk about “orthogonal reactivity,” and with good reason. If you’re planning to stitch together more complicated molecules, you want building blocks that handle tough conditions and precise transformations. I have worked with plenty of pyridine derivatives that miss the mark. Some don't play well with catalysts, some require too many protective groups, and others, frankly, don’t yield reliable results batch after batch. 3-Bromo-2-fluoropyridine tends to sidestep a lot of those issues, saving time and frustration.

    Specifications and What They Mean in Everyday Lab Work

    Looking at actual materials shipped to labs, I usually see 3-Bromo-2-fluoropyridine delivered as a colorless to pale yellow liquid or sometimes as crystalline solid, depending on the preparation and temperature. Purity matters more than the container it comes in. Reputable sources offer this product at high purities (often above 98%), ensuring that unwanted side-products or tars don’t get in the way. People in chemical research—myself included—see the impact of that purity every day: you get cleaner reactions, fewer headaches downstream, and an easier time scaling up.

    Handling it doesn't require specialized equipment beyond the usual protocols for handling halopyridines—gloves, ventilated hoods, and responsible waste management. Most labs working with halogenated aromatics already have these in place, so there’s no need for dramatic changes to the workflow.

    Making a Difference: Where 3-Bromo-2-fluoropyridine Excels

    Most of the excitement comes from applications in pharma and agrochemicals. Medicinal chemists appreciate how the fluorine atom can change metabolic stability, fine-tune electronic effects, and alter biological target binding without making the molecule unrecognizable. That can be a game-changer in trying to find a lead compound that works with the body’s complex chemistry. I know former colleagues who've shaved months off a drug discovery campaign by swapping in a fluorinated pyridine rather than rebuilding an entire scaffold from scratch.

    On the bromo side, the aromatic bromine makes it straightforward to couple the pyridine ring with other molecules. Whether it’s attaching aromatic groups for more potency or adding small alkyl chains to modulate lipophilicity, the reactions typically proceed with mild catalysts and modest heating. It’s rare to find that level of flexibility in a single intermediate.

    Agricultural innovation also gets a push from these types of building blocks. The trend has shifted toward compounds that strike just the right balance between activity and biodegradability. Fluorinated heterocycles—built, in part, from intermediates like 3-Bromo-2-fluoropyridine—show up in new classes of crop protection agents. Farmers demand tools that act precisely against pests or weeds without lingering indefinitely in the soil, and that’s where the smart chemistry comes in.

    Comparing to Other Pyridine Derivatives

    What sets 3-Bromo-2-fluoropyridine apart from its close cousins? Consider 2-bromopyridine or 3-fluoropyridine, each with just one substituent on the ring. Those are useful, especially in simpler coupling reactions, but they miss the combined advantages that a bromo and a fluoro together deliver. If you’re on the hunt for regioselectivity or planning to diversify your product at more than one site, a two-substituent scaffold offers way more control.

    Take 3-bromopyridine, for example. It comes with its own set of reactivity, but adding that fluorine at the 2-position changes everything about how the ring behaves, both chemically and in terms of downstream biological activity. The electron-withdrawing effect of the fluorine narrows down which sites react and which transformations occur, letting chemists exercise more finesse.

    On the economic side, making molecules with two substituents directly from the start—rather than doing sequential substitution—reduces the number of synthetic steps, cuts waste, and lowers the opportunity for costly mistakes. In my own experience, fewer steps mean fewer chances for something unexpected to happen. Cyanation, amination, acylation, and arylation all become more predictable, and predictability translates directly into better planning and budgeting, whether it’s for a research institution or a commercial operation.

    Supporting Innovation in Drug Discovery

    Pharmaceutical research comes down to two things: speed and reliability. The drug pipeline is crowded, competition is fierce, and delayed projects cost lives as well as resources. Choosing intermediates that are versatile, stable, and easy to adapt to late-stage modifications gives chemists more shots on goal. I remember a project where a candidate molecule kept failing final toxicity tests. With a single switch using a fluoropyridine derivative—including 3-Bromo-2-fluoropyridine as a core—researchers reopened the path and found safer analogs in short order.

    Drug designers focus on structure-activity relationships, tweaking small parts of molecules to improve their interaction with a protein or reduce off-target effects. Fluoropyridines let scientists adjust both the electronic landscape and three-dimensional structure quickly, without an overhaul of the core framework. For all the buzz about artificial intelligence in drug design, nothing beats a reliable synthetic route using well-characterized intermediates.

    Improving Environmental and Economic Footprints

    Responsible manufacturing and sustainable chemical use matter more every year. Building complex molecules with fewer steps means less solvent waste and improved energy efficiency. Many large-scale syntheses still rely on older intermediates that force chemists to use additional purification or protection steps. 3-Bromo-2-fluoropyridine often enables more streamlined approaches, curbing environmental burdens.

    Waste handling for halogenated intermediates has always been a point of concern. From my days in process scale-up, I’ve seen how minimizing reagent overuse pays off in both compliance and cost. Sourcing high-purity 3-Bromo-2-fluoropyridine means downstream reactions suffer fewer side-products, which keeps hazardous waste to a minimum. More efficient coupling steps, lower loading of catalysts, and the ability to perform selective transformations all ease the load on waste treatment facilities.

    Real-World Impact in Research and Manufacturing

    Research moves quickly, and 3-Bromo-2-fluoropyridine fits right into fast-paced workflows. Projects in pharmaceuticals or crop sciences often build on dozens of small advances compounded over years. Most of those advances rely on intermediates that deliver reliability at every step—no surprises, no batch-to-batch variation, and no incompatibility with standard laboratory equipment.

    Scale-up teams value reproducibility above almost everything. A reaction that behaves in a 10-gram flask should not fall apart when pushed to the kilogram scale. In collaborative projects, I have watched frustration boil over when otherwise promising intermediates introduced variability in crystallization, solubility, or byproduct formation. With consistent quality 3-Bromo-2-fluoropyridine, pilots and batch processes have transitioned more smoothly from lab benches to pilot plants.

    Addressing Challenges and Charting Solutions

    Every tool has limitations. Price volatility for specialty halogenated intermediates can strain budgets, especially for startups or academic labs. Companies facing this challenge have started pooling procurement power, negotiating with suppliers for more stable pricing, or establishing local custom synthesis partners.

    Exposure to halogenated aromatics brings its own safety curve. Comprehensive training, proper storage, and attention to regulatory requirements help minimize risks. An organizational culture that prioritizes continuous education for chemists and researchers can dramatically lower the chance of accidents—something I personally advocate for in any setting handling these reagents.

    Supply chain disruptions in the past have prompted some institutions to stockpile key intermediates or source them from more than one geography. Open communication with suppliers and early forecasting smooths out these bumps and keeps projects on track even when markets shift.

    Looking Ahead: Keeping Up with Innovation

    As the chemical sciences push further into complexity and precision, small molecules like 3-Bromo-2-fluoropyridine will play an increasing role. Old rules of thumb—“just start simple and substitute later”—don’t keep up with modern needs. Engineers and chemists now chase both efficacy in their target molecules and efficiency in their synthesis. I recall a time when the default was to tack on extra steps and hope for the best, but that just doesn’t cut it in competitive markets.

    Access to robust, well-characterized intermediates means new discoveries in therapeutic agents or agrochemicals actually reach the testing and approval stages faster. That creates a positive loop—better tools at the bench, more innovation, and more choices for end users in healthcare or agriculture.

    Why Experience Matters

    Trust goes beyond certificates of analysis. Having worked with unpredictable batches, off-spec materials, or questionable storage, I have learned the importance of reliable sourcing. Consistency, clear communication with suppliers, and a willingness to dig below the top level of data separate high-impact research from projects that stall out over minor setbacks.

    People in the lab remember the intermediates that perform as expected, batch after batch, allowing them to focus on discovery, not troubleshooting. 3-Bromo-2-fluoropyridine, in my experience, earns its keep not with dramatic headlines, but by enabling excellent work, day after day, for those committed to making something new or better.

    Building a Bridge to Better Chemistry

    It’s easy to overlook the quiet workhorses in chemical synthesis. Headline-grabbing breakthroughs in medicine or crop science rarely acknowledge, let alone celebrate, the small molecules that make them possible. Yet every advance needs a solid foundation. By offering a blend of practical reactivity, selectivity, and chemical stability, 3-Bromo-2-fluoropyridine stands as an example of how the right choice of building block shapes what comes next.

    Across the research landscape, the need for adaptable, high-quality reagents keeps growing. As costs, competition, and regulatory scrutiny all rise, so does the value of molecules that help scientists do more with less. 3-Bromo-2-fluoropyridine continues to prove itself in labs, pilot plants, and industrial settings, not by making the biggest splash, but by reliably powering the engine of innovation for those committed to progress.