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Methyl 6-Amino-3-Bromopyridinecarboxylate

    • Product Name Methyl 6-Amino-3-Bromopyridinecarboxylate
    • Alias MFCD11848571
    • Einecs 629-663-1
    • 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
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    Specifications

    HS Code

    714851

    Productname Methyl 6-Amino-3-Bromopyridinecarboxylate
    Casnumber 351003-22-4
    Molecularformula C7H7BrN2O2
    Molecularweight 231.05
    Appearance Off-white to light yellow solid
    Meltingpoint 82-86°C
    Solubility Soluble in DMSO and methanol
    Purity Typically ≥98%
    Storagetemperature 2-8°C
    Smiles COC(=O)C1=CN=C(C=C1N)Br
    Inchikey KWULNMJPGJWNIU-UHFFFAOYSA-N

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    More Introduction

    Introducing Methyl 6-Amino-3-Bromopyridinecarboxylate: A Versatile Intermediate for Research and Synthesis

    What Makes This Compound Stand Out in Chemical Synthesis?

    Methyl 6-Amino-3-Bromopyridinecarboxylate has emerged as an important building block for pharmaceutical and agrochemical research. Its backbone—built on a pyridine ring with amino and bromo substitutions—lets chemists pursue transformations that don’t come easy with simpler compounds. Anyone who spends time at the bench knows the aggravation of chasing after a precursor that resists modification or delivers low yields. Getting access to a reagent offering a bromine atom in the 3-position and an amino group at the 6-position means reactions like Suzuki, Buchwald, and nucleophilic substitutions become not just possible, but more direct. The methyl ester group plays its own role, making subsequent amidations or hydrolysis steps straightforward, a relief during scale-up or method optimization.

    Several years ago, while looking for step-economy routes toward new heterocyclic cores, I ran into persistent bottlenecks with old-fashioned intermediates. The molecules either demanded too many protection-deprotection cycles, or the yields suffered from selectivity issues. Shifting over to Methyl 6-Amino-3-Bromopyridinecarboxylate quietly re-shaped the approach. That’s a pattern echoed across research groups: a compound that seems ordinary at first blush ends up saving weeks of labor. Its appeal comes from convenience and reliability, which is how many innovations actually gain traction—not just on paper, but in the glassware.

    Product Details: Handling and Appearance

    This compound typically appears as an off-white or pale yellow solid, depending on the lot and trace impurities. Its structural formula features a methyl ester linked to a pyridine ring outfitted with an amino group and a bromine atom. Solubility favors polar aprotic solvents, which means it works well with DMF, DMSO, and acetonitrile. For synthetic chemists, the key is stability. This material stores with minimal sensitivity under normal lab conditions. Moisture doesn’t cause rapid degradation. Light and ambient atmosphere don’t set off decomposition. Safety guidelines for aminopyridines and bromoaromatics still apply: standard personal protective gear, local ventilation, and careful weighing avoid occupational hazards.

    Look at the model here—this isn’t just about piling on functional groups. The methyl ester brings in extra flexibility for post-synthetic modifications. It gets hydrolyzed under mild acidic or basic conditions. The amino nitrogen at the 6-position remains reactive, ready for coupling or for serving as a starting point in multistep sequences. I’ve seen a range of colleagues use different strategies, but they all appreciate time saved when pushing toward bioactive targets or new ligands. Achieving the right degree of selectivity and introducing asymmetry in later stages often becomes a matter of starting with something like this that already bears the desired handles.

    Pushing the Boundaries of Research—Where Application Meets Experiment

    It’s easy to overlook why researchers care so much about niche compounds until you’re knee-deep in a multi-step sequence and run into a wall. With Methyl 6-Amino-3-Bromopyridinecarboxylate, folks working in oncology, neurology, and crop science often turn to this kind of starting material because it allows for easy diversification. Its aromatic system provides a platform for orthogonal substitutions, which means you can fine-tune electronic or steric properties by switching out the bromine for various groups. That’s critical when you’re chasing new kinase inhibitors or designing molecules for selectivity in esoteric enzyme targets. Even outside pharma, the compound finds use as a precursor for ligands in catalysis research and in the development of novel materials for electronics.

    I remember a project in grad school where every new route started with a compromise on substitution pattern. Later work with compounds like this, with both bromine and amino groups, opened a host of options for cross-coupling. The bromo group lays a road for palladium-catalyzed reactions. The amino group at position six becomes a launchpad for peptide-like bond formation or more exotic modifications. As a result, fewer steps, reduced purification overhead, and a lower risk of side-product headaches follow. Given the cost of labor and the strategic importance of time in competitive industries like drug development, these differences can be the factor that spells success or long delays.

    Comparing With Other Pyridine Intermediates

    Not all pyridinecarboxylates offer the same level of utility. Substitution pattern makes a world of difference. Consider analogues with substitutions at the 2- or 4-positions, or ones missing the amino or bromo groups. These often require extra steps—protecting one group, transforming another, then selectively removing the protection. I once tried using an aminopyridine that lacked an activated leaving group; the reaction yields consistently disappointed, and purification chewed up precious bench time. By contrast, our compound’s profile—both a halogen ready to leave, and a primary amino group—takes much of the legwork out of finding the entry point to interesting chemistry.

    From an industrial perspective, process chemists scrutinize every extra operation added to a route. Having a precursor that tolerates storage, freezing, and thawing without rapid deterioration adds to its value. Some analogues suffer from instability or tricky purification. Crystals that need dry conditions or elaborate solvent systems to dissolve are best left for the highly specialized corners of synthesis. Working with Methyl 6-Amino-3-Bromopyridinecarboxylate sidesteps most of those obstacles.

    Quality, Testing, and the Change in Sourcing

    Chemical companies no longer take for granted that compounds simply “work” as listed. Responsible suppliers back their batches with thorough analytical data—high-resolution NMR, LCMS traces, and chromatographic purity checks. These modern standards mirror the needs of research labs wary of contaminants. Without quality verification, entire weeks of research go astray. Value in sourcing comes from consistency and clarity—knowing what you order meets the stated identity and doesn’t bring along unwanted byproducts. In my own research, more than a few plans nearly collapsed when impurities or wrong isomers snuck into the starting material. Working with suppliers committed to transparency and rigorous checks gives confidence that shows up in reproducible results.

    Lab teams expect documentation, not just a label. Spectra and certificates provide the reassurance that regulatory expectations and internal protocols remain satisfied. This differs from days past, when folks ordered by catalog code and shook their heads over variable results. The broader research community now recognizes the hidden costs of “cheap” or badly-vetted reagents. With global regulatory scrutiny growing—especially for anything destined for human or agricultural use—suppliers that invest in rigorous documentation attract repeat business not by chance, but by design. The trend is plain: as quality demands rise, so does the profile of compounds that deliver certainty as well as performance.

    The Role in Advancing Green Chemistry

    A conversation about any intermediate isn’t complete anymore without factoring in its environmental footprint. Green chemistry principles ask every process to reduce solvent use, hazardous reagents, and waste. This compound fits the trend. Because it enables efficient cross-coupling and nucleophilic substitution, researchers cut down on byproducts and avoid the need for more energy-intensive or risky operations. Some reactions relying on pyridine-based cores have shifted from multi-day, harsh-conditions syntheses to single-pot transformations, all thanks to more cleverly designed starting materials like this one.

    When I worked for a team focused on sustainable process development, it became obvious that some intermediates saved not only time but also toner on procurement forms—once lower energy or solvent requirements translated into lower emissions, the bean counters took notice. Methyl 6-Amino-3-Bromopyridinecarboxylate isn’t the only tool in this toolbox, but its compatibility with both modern catalytic systems and classical chemistry supports the drive toward greener methods in the lab and plant alike.

    Paths Toward Improvement: Addressing Sourcing and Scale-Up Challenges

    No intermediate avoids all headaches. Demand can spike overnight based on patent filings, academic breakthroughs, or supply chain hiccups in precursor chemicals. Cost remains a concern, especially as research and pilot plants ramp up to industrial scale and chase economies. Some chemists report difficulties at the kilo-scale in maintaining the same purity and batch-to-batch consistency as in gram-scale lots. A handful of my peers working in process scale-up have pointed to bottlenecks extracting or purifying this compound at larger volumes.

    Solutions aren’t limited to just finding new suppliers. Several companies now invest in process intensification—using flow chemistry or better crystallization methods to keep the quality high while scaling production. Teams have begun sharing data openly about their synthetic sequences, which supports reproducibility and helps both small-scale and industrial users troubleshoot and optimize yield. Regulatory agencies grow more attentive to trace impurities and residual solvents; integrating analytics earlier in the process turns what used to be last-minute panic into planned workflows. Coordination across suppliers, chemistry teams, and regulatory staff pays off in uninterrupted research and manufacturing timelines.

    Ideas for Moving Forward—Both in the Lab and in Policy

    It would be shortsighted to focus only on the technical side. Modern chemistry researchers increasingly ask not just how well a material performs but where it comes from, how it gets shipped, and how its lifecycle unfolds. Transparency in sourcing helps teams ensure ethical practices along every step of the chain. Upstream suppliers who follow responsible waste management and provide details about their manufacturing routes stand apart. I’ve spoken with procurement managers who—ten years ago—would have gone with the lowest bid, but now weigh environmental reporting and supplier reputation as primary factors. These changes reflect a broader cultural shift in science toward accountability.

    Training plays its part. Junior chemists who learn to work safely and efficiently with compounds like this one—understanding why certain substitution patterns pay dividends in synthetic strategy—carry those habits into industry or academia. Interdisciplinary collaboration, especially where medicinal and process chemists exchange notes on what features matter most, keeps the field moving. Professional organizations and regulators ought to standardize reporting and create open data registries so that both veteran and emerging researchers work with the best available information.

    Why Methyl 6-Amino-3-Bromopyridinecarboxylate Merits Attention

    Countless compounds claim to be breakthroughs. What sets some ingredients apart comes less from flashy marketing than from a pattern of making hard research questions a little easier to answer. Over the years, Methyl 6-Amino-3-Bromopyridinecarboxylate has earned a spot in the toolkit of synthetic and medicinal chemists for good reasons. The combination of reactivity, stability, and ease of modification offers a route through the maze of modern molecule construction.

    Its place in the market underlines a larger story—what researchers actually need in the lab, what industries ask from their supply partners, and what the next generation of sustainable and ethical chemical manufacturing will look like. Succeeding in research rarely comes from a dramatic eureka moment; more often, progress hinges on each piece of the process running smoothly. Here, having a dependable intermediate like Methyl 6-Amino-3-Bromopyridinecarboxylate means more people across academic, pharmaceutical, and industrial arenas can focus squarely on bringing new ideas to life—one reliable reaction at a time.