6-bromopyridine-2-carboxylate

    • Product Name: 6-bromopyridine-2-carboxylate
    • Chemical Name (IUPAC): Methyl 6-bromopyridine-2-carboxylate
    • CAS No.: 630423-64-8
    • Chemical Formula: C6H4BrNO2
    • Form/Physical State: Solid
    • 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

    588775

    Name 6-bromopyridine-2-carboxylate
    Molecular Formula C6H4BrNO2
    Molecular Weight 202.01 g/mol
    Cas Number 63838-10-0
    Appearance white to off-white solid
    Melting Point 120-124°C
    Solubility Slightly soluble in water
    Smiles C1=CC(=NC(=C1)Br)C(=O)O
    Inchi InChI=1S/C6H4BrNO2/c7-5-3-1-2-4(8-5)6(9)10/h1-3H,(H,9,10)
    Pubchem Cid 3468891

    As an accredited 6-bromopyridine-2-carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 6-bromopyridine-2-carboxylate comes in a 5g amber glass bottle with a tamper-evident cap and clear labeling.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 6-bromopyridine-2-carboxylate ensures secure, compliant bulk packaging, maximizing space for efficient, safe chemical transport.
    Shipping 6-Bromopyridine-2-carboxylate is shipped in tightly sealed containers to prevent moisture and contamination. It is packaged according to safety regulations for hazardous organic chemicals, typically padded and labeled with appropriate hazard symbols. During transit, it is protected from heat, direct sunlight, and strong oxidizing agents to maintain product integrity.
    Storage 6-Bromopyridine-2-carboxylate should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed when not in use. Store in a chemical storage cabinet, preferably under inert atmosphere or nitrogen if sensitive to moisture or air. Ensure appropriate labeling and access only to trained personnel.
    Shelf Life **6-Bromopyridine-2-carboxylate** typically has a shelf life of 2-3 years if stored in a cool, dry, tightly sealed container.
    Application of 6-bromopyridine-2-carboxylate

    Purity 98%: 6-bromopyridine-2-carboxylate with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency.

    Melting point 128°C: 6-bromopyridine-2-carboxylate featuring a melting point of 128°C is used in organic synthesis reactions, where thermal stability is critical for controlled processing.

    Particle size <10 µm: 6-bromopyridine-2-carboxylate with particle size under 10 µm is used in catalyst preparation processes, where increased surface area enhances reaction rates.

    Moisture content <0.3%: 6-bromopyridine-2-carboxylate with moisture content below 0.3% is used in high-precision analytical studies, where minimized water interference improves reproducibility.

    Stability temperature up to 60°C: 6-bromopyridine-2-carboxylate stable up to 60°C is used in storage and transport logistics, where the prolonged shelf life is required.

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    Certification & Compliance
    More Introduction

    6-Bromopyridine-2-Carboxylate: A Fresh Take on Pyridine Chemistry

    Scientists and chemical engineers have long turned to pyridine derivatives as reliable workhorses in research and synthesis. 6-bromopyridine-2-carboxylate stands out not only for its unique molecular structure but also for the growing interest around its versatile performance in both lab and industry settings. If you’ve spent any time at the bench, fiddling with reaction conditions or looking for that right building block, you know the frustration that comes from unpredictable intermediates. This compound has caught the attention of both academic teams and commercial users for several reasons, most notably its role as a finely tuned intermediate in crafting complex molecules.

    Understanding the Basics: What Sets This Molecule Apart

    It’s easy to lump every halogenated pyridine into a single basket, but 6-bromopyridine-2-carboxylate brings some extra value. Here, the position of the bromine at the 6-spot matters more than some realize. When the bromine sits at position 6 on the pyridine ring and you tack a carboxylate at position 2, you’re setting up reactivity that can shift the direction of a whole synthetic pathway. For organic chemists, selectivity matters, and the specific placement on this scaffold lends itself to transformations you can’t always pull off with the more commonly used 3- or 4-substituted pyridines. Whether you run Suzuki couplings, try nucleophilic substitutions, or think ahead toward late-stage functionalization, having a bromo at the 6-position offers a gateway to more targeted modifications.

    In research, reproducibility and purity sit at the center of every successful project. 6-bromopyridine-2-carboxylate comes in as a high-purity crystalline solid, often showing a reliable melting point and good solubility in solvents most chemists already trust. No one wants to lose days debugging side reactions caused by unknown impurities, and clean starting materials save time. As someone who’s spent too many evenings in the lab chasing down unexplained NMR peaks, I see the peace-of-mind advantage a reliable supply brings.

    From the Bench to the Plant: Where Chemists Put it to Work

    Building heterocycles and medicinal scaffolds means walking a tightrope. You want complexity, but you want control and predictability. In drug discovery—where time means everything—this molecule has proven its value as a stepping stone. Medicinal chemists often look for ways to introduce new polar groups or to make rapid changes at key parts of an aromatic ring. The 6-bromo handle means you can leverage modern palladium-catalyzed cross-coupling chemistry, opening doors to a wide variety of derivatives, each suited for a different biological target. That kind of flexibility is gold.

    Process chemists don’t just focus on what works in a tiny flask. Once the target molecule shows promise, teams face the challenge of scaling up. Unpredictable side reactions grow worse as batch size jumps. 6-bromopyridine-2-carboxylate supports both R&D scaleups and routine production, holding onto purity even on larger runs. This kind of reliability matters as folks in the API business shift from grams to kilograms.

    Its applications continue beyond pharma. Agrochemical researchers draw from the broad toolbox of halogenated pyridines for crop-protection studies, seeking structures that keep selectivity high while remaining accessible to large-scale manufacturing. You’ll notice the trend: chemists keep coming back to manageable intermediates that combine easy handling with robust downstream chemistry.

    Specifications: Details That Matter

    Discussing features gets dry quick, but let’s stick to what matters for those who actually use this molecule. Most reputable sources deliver 6-bromopyridine-2-carboxylate in fine crystalline form, pale yellow or off-white in color, which offers practical advantages when weighing or dissolving. You’ll find strong solubility in typical organic solvents—DMF, DMSO, acetonitrile, even common chlorinated hydrocarbons. In practice, you won’t spend hours coaxing it into solution or worrying about persistent clumping.

    A common bottleneck in heterocyclic synthesis? Difficult purification. This carboxylate tends to behave during column chromatography, largely thanks to the electron-withdrawing bromine and carboxylate groups, which help separate your compound from starting materials and typical byproducts. The melting point hovers within a range that suggests high purity, and the product holds up well under standard dry storage conditions. Chemical suppliers sometimes get lost in numbers and metrics; anyone who’s made do with sticky, clumpy solids appreciates an intermediate that keeps its form over time.

    Drawing Key Differences

    It’s tempting to reach for whatever pyridine derivative sits on the shelf, but comparing one to another unlocks subtle advantages. 6-bromopyridine-2-carboxylate distinguishes itself from its cousins on two fronts: functional diversity and reaction control. Compare it with 2-bromopyridine, lacking that carboxylate, and you lose the directing effect in target couplings. Choose 2-chloropyridine-6-carboxylate and you’ll find fluoride chemistry less straightforward and leaving groups less reactive in cross-couplings.

    Years of synthetic work have shown that bromo-substituted aromatics generally outperform chloro- or fluoro-analogs when you need them to leave cleanly in metal-catalyzed coupling reactions. Palladium catalysis, the backbone of modern ligation chemistry, hands the advantage to bromides, especially when high yields and short reaction times make a difference. The presence of a carboxylate, meanwhile, lets you branch out into amide, ester, and acid chloride chemistry with little extra effort. One molecule, and suddenly you’re not chasing down niche reagents or troubleshooting step after step.

    It’s also worth thinking about cost-of-goods and handling. Some derivatives with extra nitro or amino groups call for careful handling under inert atmosphere or demand expensive stabilizers just to sit on a shelf. In contrast, 6-bromopyridine-2-carboxylate stores easily in a dry bottle, and most run-of-the-mill chemical operations aren’t disrupted by specialized requirements. As cost pressures intensify and labs juggle larger numbers of projects on tighter budgets, the practical, stable stock wins the day.

    Looking Past the Molecule—Why its Popularity Keeps Rising

    Researchers often talk about molecular innovation, but in day-to-day practice, convenience takes top priority. When I review literature or catch up with colleagues, a pattern emerges: the compounds most often cited aren’t always groundbreakers, but they’re accessible, reliable, and get the job done. The trend for 6-bromopyridine-2-carboxylate maps onto this reality. With so many teams working on new small molecules—whether for human health, plant science, or material research—having intermediates that combine reactivity, availability, and user-friendly handling keeps projects moving forward.

    Academic labs, under pressure to publish and juggle training students, benefit from reagents that perform as expected. Industry teams, saddled with compliance and quality audits, turn to materials that meet spec every time. It’s easy to overlook these under-the-radar building blocks, but success in synthetic chemistry so often boils down to reliable steps and access to well-characterized intermediates. During the post-pandemic boom in small-molecule research, fluctuations in supply chains put even simple building blocks under the microscope. Single-source dependence or sporadic stockouts throw project timelines out of sync; that’s why researchers favor robust intermediates like this one, which are reliably restocked by multiple vendors.

    It’s not only drug discovery that benefits. Materials scientists, working to construct electronic polymers or advanced dyes, need building blocks with robust electron-withdrawing capacity. The carboxylate and bromo together allow tailored functionalization options without creating roadblocks later in the synthesis. In some published material, this combination has opened up surprising possibilities in high-performance electronics and advanced imaging chemicals.

    Scale-Up, Sourcing, and the Supplier Landscape

    Building a solid project pipeline requires more than just clever lab tricks—it also depends on sourcing intermediates that won’t hold back a team once demand grows. 6-bromopyridine-2-carboxylate, thanks to increasing demand, now sees manufacture in both specialty and larger-batch settings. That puts quality assurance and batch-to-batch consistency center stage. Considering my own experience, early-stage projects often meet setbacks because initial R&D samples don’t match the larger batches dispatched for pilot runs.

    Quality control teams now look for suppliers who can document process control and deliver solid analytics. Here, established sources run NMR, HPLC, and elemental assays to confirm identity and purity. Spot checks for residual solvents and controlled drying eliminate the headaches caused by unpredictable batches. Clean certificates of analysis instill trust, especially when your next synthetic step demands threshold performance.

    Sourcing also overlaps with safety and regulatory compliance. Some pyridine derivatives see inconsistent regulation around the world, particularly with halogenated or nitro-aromatics. 6-bromopyridine-2-carboxylate occupies a middle ground where the hazards align with standard lab procedures. Users report straightforward hazard communication, clear labeling, and compatibility with typical waste treatment protocols.

    Looking deeper at the global market, broad adoption keeps pressure on suppliers to maintain competitive pricing, ensure robust supply lines, and provide prompt technical support. Gone are the days where a reactive intermediate trickled out of only one boutique lab; today’s research ecosystem leans hard on distributed manufacturing and scalable quality. Scientists benefit from this fierce competition, gaining access to fresh batches with detailed analytical backup, and prompt shipping to limiting down time.

    Bridging the Lab–Industry Divide: Realistic Application

    Skeptics sometimes ask if one intermediate really makes a difference, but the answer often comes out in the details. Researchers across pharma, agriculture, and materials echo a similar refrain: access to quality building blocks speeds up innovation. Putting myself in the shoes of a medicinal chemist or a chemical engineer, I recognize that the product’s flexibility matters most not on the brochure or data sheet, but out on the line, where a stuck batch or failed scale-up ruins workflows and affects downstream deliverables.

    Companies that tap into the potential of 6-bromopyridine-2-carboxylate give themselves a smoother ride through route scouting and lead optimization. Unlike more tightly regulated or unstable pyridine compounds, this one remains stable through rounds of storage, shipment, and use. It’s rare that an intermediate brings together ease of use, purity, and broad applicability. More often, you’re forced to compromise, but many have found that this compound hits that practical sweet spot.

    For process chemists, the reduction in steps and the cleaner reaction profiles mean lower solvent use and easier purification. In the era of green chemistry, even modest gains in efficiency add up, cutting both direct costs and the hidden price of waste management. As environmental accountability grows, so does interest in intermediates that perform reliably without generating piles of hazardous waste. 6-bromopyridine-2-carboxylate’s ready fit for cross-coupling chemistry means people can abandon toxic organotin or organomercury reagents, which were once common but now get flagged by safety and environmental offices.

    Innovation Pushed by Real Needs: What the Community Sees Next

    Research communities have a knack for pushing every tool in the box further than its original intent. With drug discovery racing ahead—thanks to machine learning, structure-based design, and evolving high-throughput chemistry—the demand for adaptable intermediates doesn’t slow down. 6-bromopyridine-2-carboxylate has moved beyond a niche role as more teams realize the power of late-stage diversification. In fragment-based drug design, narrow windows of selectivity make the difference between compounds that reach animal testing and those that stall out. Here, the molecule’s reactive bromine and functional carboxylate combination allow for rapid expansion of lead-like diversity.

    Agrochemical labs, similarly, now rely on modularity—taking a single intermediate through dozens or even hundreds of analogues, each tweaked for insect, weed, or fungal targets. With climate change adding pressure for new crop protections, fast-turnaround chemistry saves valuable time. Experiences from conferences and trade journals confirm that having the right intermediate on hand can make a whole campaign run smoother.

    Not every trend is positive. Growth in demand sometimes fuels supply challenges, counterfeit stocks, or inconsistent quality from fly-by-night vendors. This reinforces the value of supplier vetting, community communication, and building direct relationships with trusted manufacturers. Lessons from the pandemic era still ring true—secure logistics and order planning, not the lowest possible price, keep projects on track.

    What Could Improve—Ongoing Challenges

    No product is perfect. One challenge for many users emerges around waste management. Even though 6-bromopyridine-2-carboxylate itself isn’t flagged as unusually hazardous, reactions that use it—especially when run at scale—still generate byproducts and contaminated solvents requiring clear disposal strategies. Green chemistry initiatives urge manufacturers and labs to improve yield, minimize halogenated solvent use, and streamline workup. Some promising work points toward using water-based purification or developing catalyst systems that let you run these reactions cleaner, with fewer additives.

    Cost will always come up in conversations with purchase departments and project leaders. With recent swings in basic pyridine and halogen source markets, prices aren’t always as stable as budgets require. Teaming up with reputable vendors and keeping an open line for forecasting and lead-time coordination offers some insulation against shocks.

    Sustainability also deserves attention. New research pushes for more renewable input streams—not all pyridine-based products trace their origins back to green or bio-based feedstocks. The day might come when regulatory pressure or shifting market values require intermediates like this one to pivot to more sustainable supply chains.

    Community Knowledge and Real Experience

    Having spent years swapping tips with colleagues in both small academic labs and sprawling industrial sites, I can say with confidence that intermediates like 6-bromopyridine-2-carboxylate represent more than just a line-item chemical. People develop a sense of trust around materials that deliver. Community forums buzz with advice about reaction tweaks, insights on purification, and troubleshooting around batch differences. Experienced chemists recognize the stress that comes from a failed step caused by a bad batch, and regularly share advice on both verification and storage.

    Some users cite the importance of keeping incoming stock dry and away from light, at least for long-term storage, especially in humid environments. Others point out that trace hydrobromic acid formation—though rare—can affect sensitive reactions, so confirming the absence of such contaminants shows up in quality-control routines. These habits, built from years of experience and collective wisdom, remind us that even the best reagent rewards those who handle it with care.

    Conclusion: The Value of a Reliable Intermediate

    Every bench scientist knows the quiet satisfaction of reaching for a trusted bottle and moving a reaction forward, step by step. 6-bromopyridine-2-carboxylate occupies just such a place in the toolkit of modern chemistry, linking classic heterocyclic synthesis with the evolving priorities of green chemistry, global supply reliability, and targeted innovation. Its popularity won’t wane as long as users keep demanding dependable, multifaceted intermediates that support discovery and development across disciplines. As research leans harder into efficiency, scale, and sustainability, practical compounds like this one look set to remain in high demand—quietly fueling the breakthroughs of tomorrow.