2-Methoxy-3-chloro-5-bromopyridine

    • Product Name: 2-Methoxy-3-chloro-5-bromopyridine
    • Chemical Name (IUPAC): Sorry, you did not specify a product. Please provide the name or structure of the product.
    • CAS No.: ''
    • Chemical Formula: ''
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    Specifications

    HS Code

    191002

    Product Name 2-Methoxy-3-chloro-5-bromopyridine
    Molecular Formula C6H5BrClNO
    Molecular Weight 222.47 g/mol
    Cas Number 886373-74-0
    Appearance Light yellow to brown solid
    Melting Point 49-53°C
    Purity Typically ≥98%
    Solubility Slightly soluble in organic solvents such as DMSO, DMF
    Smiles COC1=NC(=C(C=C1Br)Cl)
    Storage Temperature 2-8°C
    Synonyms 3-Chloro-5-bromo-2-methoxypyridine

    As an accredited 2-Methoxy-3-chloro-5-bromopyridine 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 2-Methoxy-3-chloro-5-bromopyridine, tightly sealed, labeled with hazard and product information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 2-Methoxy-3-chloro-5-bromopyridine: Securely packed in sealed drums, compliant with safety and international shipping regulations.
    Shipping 2-Methoxy-3-chloro-5-bromopyridine is shipped in sealed, chemically resistant containers to prevent contamination and degradation. It is handled as a hazardous material, following relevant transport regulations, including proper labeling and documentation. Shipping may require temperature control and is typically conducted by certified carriers, ensuring safety and regulatory compliance throughout transit.
    Storage Store 2-Methoxy-3-chloro-5-bromopyridine in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers and acids. Keep container tightly closed when not in use. Ensure proper labeling and store at recommended temperatures, typically room temperature unless otherwise specified by the manufacturer or safety data sheet.
    Shelf Life 2-Methoxy-3-chloro-5-bromopyridine is stable under recommended storage conditions; shelf life is typically several years if kept dry, cool, sealed.
    Application of 2-Methoxy-3-chloro-5-bromopyridine

    Purity 98%: 2-Methoxy-3-chloro-5-bromopyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurity formation.

    Stability temperature 120°C: 2-Methoxy-3-chloro-5-bromopyridine with stability temperature 120°C is used in high-temperature organic transformations, where it maintains chemical integrity and consistent reaction outcomes.

    Melting point 60–62°C: 2-Methoxy-3-chloro-5-bromopyridine with melting point 60–62°C is used in solid-phase synthesis, where it allows precise thermal control and reproducible melting behavior.

    Molecular weight 238.46 g/mol: 2-Methoxy-3-chloro-5-bromopyridine with molecular weight 238.46 g/mol is used in agrochemical development, where accurate dosage calculation and formulation consistency are achieved.

    Particle size <50 µm: 2-Methoxy-3-chloro-5-bromopyridine with particle size less than 50 µm is used in catalytic applications, where enhanced dispersion and surface reactivity improve catalytic efficiency.

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    Certification & Compliance
    More Introduction

    Redefining Precision Chemistry: Introducing 2-Methoxy-3-chloro-5-bromopyridine

    Grounded Innovation in Fine Chemical Synthesis

    As someone who’s spent years watching chemists weigh out reagents with steely focus, there’s one thing that stands out again and again: the best results come from coupling scientific rigor with imaginative thinking. 2-Methoxy-3-chloro-5-bromopyridine lands right in the middle of that sweet spot. Here we have a compound that isn’t just a trick pulled out of a textbook; it’s got the flexibility researchers and manufacturers keep hunting for in the lab and on the bench.

    The chemical structure on display here—a pyridine ring sporting methoxy, chloro, and bromo groups—offers both selective reactivity and a platform for tailoring new molecules. That’s a big deal in the world of heterocyclic chemistry. The 2-methoxy handle changes electron distribution, setting up the pyridine to react in ways pure pyridine can’t. The chlorine and bromine open doors for cross-coupling and further substitutions. With this arrangement, chemists can build up complexity in streamlined steps, saving precious time and reducing waste.

    The Specifics: What Sets This Molecule Apart

    Let’s get into the nuts and bolts. 2-Methoxy-3-chloro-5-bromopyridine typically comes as a white to pale yellow powder, easy to observe for purity as it moves through a synthesis. You can often pick out trace impurities with HPLC or NMR, which is critical for work in medicinal chemistry or when making electronic materials. Boiling point and melting point data (usually found in open literature reports on this compound) support reliable and repeated processing. Chemists frequently demand analytical data—provenance for every lot—so reputable manufacturers back this compound with detailed COAs, listing NMR, mass spec, and elemental analyses.

    Unlike a lot of generically halogenated pyridines, adding methoxy at the 2-position brings a balance of electron-rich and electron-withdrawing properties. This balancing act encourages certain selectivities in Suzuki, Stille, or Buchwald-Hartwig reactions. In my own experience working on heterocyclic scaffolds, this extra functionalization really means you can modify the core stepwise, building larger molecules piece by piece with more certainty that the rest of the pyridine won’t react where you don’t want it to. That’s cheaper and safer—less surprise and less waste.

    Tangible Impact on Research and Industry

    People in drug discovery, especially, keep searching for unusual starting materials to drive up molecular diversity during lead optimization. All those functional groups on 2-Methoxy-3-chloro-5-bromopyridine set it up for creative syntheses. Want to attach an aryl group at one position, leave another ready for a different nucleophile, or crank up the polarity for better solubility in water or DMSO? This compound gives a clear route. For anyone looking at SAR (structure-activity relationship) studies, having access to this scaffold enables direct analog generation—test out new biologically active molecules without constantly going back to square one on the synthesis.

    In the area of advanced materials, p-type and n-type dopants feed into organic electronics and polymer chemistry. Building blocks like 2-Methoxy-3-chloro-5-bromopyridine come in handy for functionalizing thin films, OLED layers, and sensors. Its robust halides anchor key reactions in the preparation of more complex structures, while the methoxy substitution tweaks solubility or shifts absorption profiles, sometimes making all the difference between an average sensor and a best-in-class device. Chemists and engineers track how minute changes in molecular structure push forward next-generation materials.

    How It Compares to Other Pyridines

    A lot of halogenated pyridines look similar on paper. The difference lies in how those functional groups tune the reactivity and downstream pathways. Regular 3-chloropyridine or 5-bromopyridine lack the flexibility delivered by the methoxy group. Methoxy not only pumps electrons into the ring, it changes how other groups interact across the molecule. The combined halide groups—chlorine and bromine—open parallel strategies for cross-coupling; for instance, bromine can go through palladium-catalyzed arylation, whereas chlorine offers more cost-efficient, though less reactive, coupling under the right ligands.

    This mix of reactivity isn’t just theoretical. In practice, competing products either give high selectivity on one position, or require extra protection-deprotection steps in a synthetic pathway. Each extra step adds cost and introduces the risk of lower yields or unwanted side products. Using 2-Methoxy-3-chloro-5-bromopyridine, I’ve seen synthetic routes tighten up fast—fewer stages, cleaner extracts, simpler purification. In one medicinal chemistry project, what used to take four step modifications dropped to two, giving room to test more analogs and push forward on project timelines. Productivity counts in high-stakes discovery projects.

    Supporting Quality Through Traceability and Testing

    Scientific credibility hinges on reliability. Any fine chemical—especially one with multiple halides and a heterocycle—commands close attention to trace metal content, residual solvents, and handling stability. Labs focused on new molecule creation don’t gamble on mystery lots. For 2-Methoxy-3-chloro-5-bromopyridine, I look for suppliers with transparent records and batch-specific documentation. A solid COA includes not just main spectral data (1H NMR, 13C NMR, LC-MS), but updates on any trace impurities, shelf stability data, and often even residual heavy metal content, since those can quietly poison a whole campaign if left unchecked. Patients, regulatory bodies, and fellow scientists count on these checks—and so do careers built on successful research.

    Testing at both the supplier and laboratory levels reinforces confidence. For projects at scale, quality teams run confirmation NMR and purity checks before a batch ever enters production. If a deviation shows up at any stage, that saved time and resource loss is huge, compared to blindly trusting an untested batch. I’ve learned through long hours in the lab: the closer you stay to the analytical data, the faster issues get resolved, with less downstream headache and firefighting.

    The Role of Responsible Sourcing and Environmental Safety

    Ethical sourcing increasingly shapes choices around specialty chemicals. Brominated and chlorinated compounds, while essential for research, need careful stewardship. Researchers and purchasing managers face real questions on waste handling and lifecycle impacts. Disposal routes for leftover halogenated solvents and residues follow stricter protocols than ever before. In my own experience working with campus environmental teams, failure to handle waste right leads to expensive cleanups and undermines both trust and compliance. Responsible suppliers help relieve some of the burden, shipping product with clear safety guidelines and sustainable practices.

    Some innovators have started using green chemistry to reduce emissions during synthesis of building blocks like 2-Methoxy-3-chloro-5-bromopyridine. Greener routes may cut production’s environmental toll, or lower the risks of residual toxic byproducts. These efforts don’t just meet regulations—they open markets. Pharma and high-end material producers increasingly audit upstream supply chain practices for both compliance and reputational risk. When a chemical demonstrates traceability back to a responsible source, buyers can rest easier, knowing their projects avoid hidden environmental costs.

    Unlocking New Synthetic Pathways

    At its core, this compound is about options. Synthetic chemists love materials that encourage creative planning. That’s exactly what having multiple reactive groups enables: you map shorter, more diverse routes, shifting a strategy on the fly to chase an unexpected result or pivot away from a failed step. I’ve seen research teams switch directions mid-project, salvaging value from what might have been a dead end. Pyridine derivatives like this enter the stage as multi-purpose tools—no need to start from scratch with each new analog.

    Some routes take advantage of the bromo substituent for cross-coupling, while others go after the chloro group under more forcing conditions. With the 2-methoxy twist, conversions that would normally produce messy mixtures in raw pyridine derivatives go smoother. You can direct transformations precisely, stepping through Suzuki or Buchwald-Hartwig procedures at distinct positions, then polish up the final molecule with targeted deprotection or functionalization. Every saved synthetic step translates directly into lower resource use and higher safety in scale-up environments. Beyond the obvious reductions in hazardous waste, fewer steps often mean fewer bottlenecks and more predictable scheduling.

    Solving Practical Lab and Production Challenges

    Practical issues pop up in every stage of chemical handling, from procurement to pilot plant. Some pyridine salts and halogenated intermediates only store well under inert gases, risking rapid decomposition. The stable crystalline form of 2-Methoxy-3-chloro-5-bromopyridine stands up better in ambient storage, reducing loss due to hydrolysis or oxidation. This gives both bench chemists and warehouse teams more flexibility—less special packaging, more predictable reordering. Reliable shelf stability ties back into safer lab practices. Chemists don’t have to gamble between using fresh stocks and taking a risk on something that’s quietly degraded on the shelf.

    Handling safety matters just as much. Exposure risks tend to scale with volatility of the compound, purity of solvent, and local ventilation. As with all halogenated pyridines, 2-Methoxy-3-chloro-5-bromopyridine asks for basic measures: gloves, proper eyewear, fume hoods for transfer and weighing. In multi-ton production, well-designed process hazard analyses catch most issues before scale-up, especially concerning generation of acidic or noxious byproducts during high-temperature reactions. In smaller labs, clear labeling and safe storage get more respect than any abstract set of safety guidelines.

    Meeting Tomorrow’s Research Demands

    Solid specialty intermediates become the foundation for projects that might change the way we treat disease, store energy, or sense the physical world. As scientific fields blend more disciplines—combining synthetic organic chemistry, material science, and molecular biology—engineers keep hunting for advanced scaffolds that allow modifications both at the molecular and functional level. Having a reliable, reactive, and customizable building block saves time, money, and effort.

    2-Methoxy-3-chloro-5-bromopyridine’s role doesn’t end in pilot projects. As startup teams move from research to manufacturing, they have tough scale-up and tech transfer requirements. The same functional versatility that enables R&D success must stick through kilo-lot or commercial batch production—with tight controls on impurity profiles and streamlined logistics. Modern supply chains are just as demanding as regulatory agencies or funding boards; bottlenecks, delivery delays, or downgrades in purity ripple out fast. Solid partnerships with reputable chemical suppliers—grounded in transparency and real data—act as insurance against these setbacks. Experience in the trenches has shown me again and again: the right starting materials mean fewer headaches at launch.

    Opportunities and Directions for the Next Decade

    A fine chemical’s journey from research reagent to industry mainstay travels through cycles of feedback. Medicinal chemists prize these functionalized pyridines for testing out SAR hypotheses. Polymer engineers harness them to add function without losing strength or durability. Analytical teams rely on clean spectra for both process monitoring and troubleshooting. As markets shift—whether with tighter purity expectations, greener procurement, or sped-up innovation cycles—the full potential of 2-Methoxy-3-chloro-5-bromopyridine stands to grow.

    I see ongoing demand for new analogs tailored to specific applications, as regulatory and technical challenges evolve. Green chemistry will keep shaping synthetic methods, aiming to cut waste, emissions, and toxic byproducts at every step. Suppliers that adapt to this push—and chemists who collaborate openly with their sources—will open new paths for safe, scalable, and cost-effective innovation. The biggest wins go to labs that keep an open channel to the scientists upstream: sharing not just problems, but lessons learned from real-world failures and breakthroughs.

    Supporting Breakthroughs in Discovery and Application

    Stepping back, what excites me most isn’t the technical data or the purity percentages; it’s the practical results. Every year, new therapies, smarter materials, and more responsive sensors hit the market, built in part from carefully chosen fine chemicals. The art sits in selecting the right material for a challenge. Research groups landing the next big deal in molecular medicine, or industrial teams fine-tuning energy storage, often point back to “one crucial intermediate” that made the difference between stalled ideas and tangible progress.

    I’ve watched teams with limited budgets do more—faster—by cutting out redundant steps, harnessing the flexibility in a scaffold like 2-Methoxy-3-chloro-5-bromopyridine. Rather than pouring funds into long, tedious synthesis, they invest time in testing and optimization. This feedback loop of synthesis, test, and redesign looks simple, but without robust building blocks, it grinds to a halt. That’s where high-value intermediates prove their worth, sparking discovery and, ultimately, broader access to novel solutions.

    Reflecting on Value: Beyond The Bench

    For all the focus on building ever-more complex molecules, the foundation remains: quality inputs unlock better science. 2-Methoxy-3-chloro-5-bromopyridine doesn’t promise a silver bullet, but—like many prized building blocks—it gives teams a reliable way to explore, modify, and scale up new chemistry. In my experience, that consistency makes all the difference, both for researchers setting out new pathways and for companies looking to push products ahead of the curve. While trends in chemical manufacturing keep changing, the demand for trustworthy, well-characterized reagents endures. In these moments, the blend of creativity, diligence, and practical experience shapes tomorrow's breakthroughs.