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4-Bromopyridine-2-Carboxamide

    • Product Name 4-Bromopyridine-2-Carboxamide
    • Alias 4-bromo-2-pyridinecarboxamide
    • Einecs 609-411-7
    • 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

    223513

    Chemical Name 4-Bromopyridine-2-Carboxamide
    Molecular Formula C6H5BrN2O
    Molecular Weight 201.02 g/mol
    Cas Number 114772-54-2
    Appearance White to off-white solid
    Melting Point Approximately 150-155°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Boiling Point Decomposes before boiling
    Synonyms 2-Caboxamid-4-bromopyridine
    Storage Conditions Store at room temperature, keep tightly sealed
    Smiles C1=CC(=NC=C1C(=O)N)Br
    Inchi InChI=1S/C6H5BrN2O/c7-4-1-2-8-5(3-4)6(9)10/h1-3H,(H2,9,10)

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    More Introduction

    Introducing 4-Bromopyridine-2-Carboxamide: Why It Matters in Modern Chemistry

    An Up-Close Look at 4-Bromopyridine-2-Carboxamide

    Chemistry relies on building blocks, and few stand out as much as 4-Bromopyridine-2-Carboxamide in research and synthesis labs. I’ve worked with a variety of heterocyclic compounds, but this one often forms the backbone of vital developments in pharmaceuticals and organic materials. Traditionally, labs have gravitated toward well-known reagents for pyridine ring synthesis, usually sticking with the tried and true. Lately, innovation has been pushing boundaries, giving researchers better building blocks for creating new molecules. This compound, topped with a bromine atom at the four-position and a carboxamide group at the two-position, shows its value in those contexts.

    Why 4-Bromopyridine-2-Carboxamide Stands Out

    For anyone immersed in synthetic work, versatility keeps projects moving. The molecular structure here features a pyridine ring, which for decades has been central for medicinal and material chemistry: easy for skilled hands to modify and tough enough for further transformations. Efficiency on the bench increases, because the bromo and carboxamide groups let researchers change pathways quickly. 4-Bromopyridine-2-Carboxamide brings together halogenation and amidation, creating more routes for creating drug candidates or fine-tuning intermediates.

    The bromine atom finds use as a leaving group in cross-coupling reactions. Over the past several years, Suzuki-Miyaura and Buchwald-Hartwig couplings have given plenty of chemists access to complex, otherwise hard-to-make molecules. Unlike versions of pyridine that have chlorine or iodine in the same spot, the brominated version provides solid balance. I’ve found that chlorine can drag down reactivity in some cases, forcing you to use higher temperatures. Iodine brings reactivity but hikes up costs and sometimes brings purity headaches. Here, bromine gives chemists the best of both worlds: fast reaction rates, manageable cost, and good selectivity.

    But the amide group adds another layer. I’ve often reached for it when aiming to graft small molecules or stabilize functional groups prone to breakdown. The carboxamide moiety typically resists hydrolysis and oxidation, so batches last longer on the shelf without losing punch. Handling becomes far less stressful compared to nitriles or esters, which can give off unwanted smells or break apart too easily during complicated syntheses.

    Practical Application in Pharmaceutical Synthesis

    Several recent drug development projects have drawn from 4-Bromopyridine-2-Carboxamide to speed up early-stage testing. The backbone often appears in kinase inhibitors or emerging antibiotic scaffolds. Having a stable, modifiable compound at hand helps accelerate hit-to-lead optimization. In one research environment I watched, our group needed to stitch new aryl fragments onto a pyridine ring—using a Suzuki coupling with palladium as the catalyst. Turning to the brominated carboxamide delivered more consistent yields, even when we tried to scale up from milligrams to grams. Contaminants from incomplete reactions stayed low, easing purification. That’s a direct saving in time and material costs.

    It also helps that the compound dissolves easily in the main organic solvents—DMF, DMSO, and acetonitrile—without the lengthy sonication or heating you often find necessary with less soluble pyridines. Solubility may seem like a minor issue, but in reality, it often dictates whether a synthetic campaign stays on track or stalls for weeks. Reliable solubility translates into smoother reaction monitoring by NMR and HPLC, and that means fewer repeats or surprises with analytical data.

    Comparing Against Similar Reagents

    Plenty of pyridine derivatives sit on shelves in research labs—2-aminopyridine, 4-chloropyridine, and the methylated variants all have their fans. Still, 4-Bromopyridine-2-Carboxamide stands apart due to its two active sites: bromine and carboxamide. The majority of off-the-shelf pyridines offer either a single site for modification or lack the amide’s stability. In practical terms, this means fewer protection and deprotection steps, which lets teams move faster from initial design to preliminary biological testing.

    Having handled both 4-bromo and 4-chloropyridine analogues in parallel projects, the jump in coupling efficiency is hard to ignore. Chlorides put up more resistance, often demanding longer reaction times or more expensive ligands, while bromides like this one give faster turnover with mainstream catalysis systems. For labs running on tight budgets and timelines, that difference compounds over the course of a project.

    Modifying the carboxamide group offers additional appeal. Some aromatic carboxamides can participate in hydrogen bonding, letting researchers tweak solubility and biological properties as projects advance. I’ve watched medicinal chemists exploit this in fragment-based drug discovery, switching out the amide for tailored groups that bring about sharper structure-activity relationships.

    Sourcing and Purity: What’s Worth Watching

    Grabbing a batch of 4-Bromopyridine-2-Carboxamide from a reputable supplier matters more than price points alone suggest. From my own ordering experiences, purity levels above 98% save more trouble down the line than a lower upfront invoice. Minor byproducts, like dihalogenated species or unreacted starting material, can throw off sensitive reactions or complicate scale-up. Companies who document their synthetic route and provide robust batch-to-batch testing tend to deliver a product that won’t trigger headaches during quality control checks.

    Paying close attention to moisture content helps as well. Carboxamides can sometimes absorb water, leading to sluggish reactions or the need for extra drying before use. Analytical data like NMR, MS, and HPLC profiles add peace of mind, offering quick confirmation that the chemical will work as expected every time.

    Handling and Storage: Small Details, Big Savings

    On a practical level, I’ve always appreciated stable solids over oils or low-melting crystals. 4-Bromopyridine-2-Carboxamide stores easily at room temperature, kept away from direct sunlight and humidity. Contrast this with some more volatile pyridines or analogs, which can require refrigeration or even inert atmosphere storage to hang onto potency. Shelf stability keeps workflows flexible—no interrupted schedules because a sensitive intermediate degraded before it could be used.

    Material that doesn’t clump, decompose, or take on water as soon as the container opens provides more consistency batch after batch. I’ve noticed bulk containers maintain flow characteristics for months, rather than turning into bricks overnight. Every researcher values compounds that cooperate in the real world, not just on a spec sheet.

    Environmental Considerations in Modern Labs

    Increasingly, green chemistry has become a touchpoint for purchasing and process design. Traditional halogenated aromatics sometimes draw environmental scrutiny—nobody wants to become known as the source of hazardous waste issues. As I’ve seen in sustainability initiatives, bromine-containing intermediates like 4-Bromopyridine-2-Carboxamide slip comfortably into protocols designed for safe handling and disposal. Most major safety guidelines cover procedures for brominated pyridines, and their waste streams can be treated alongside similar materials.

    Switching to this compound over others with more toxic halogens or less stable side chains lets labs cut down on both workplace hazards and environmental footprints. Modern waste treatment facilities offer validated methods for neutralizing bromide ions. Automated systems in research settings help trap and separate halogenated byproducts before they make their way into shared waste containers. The predictable behavior of this molecule under typical laboratory conditions helps ensure that a researcher’s attention can stay focused on innovation, instead of emergency response.

    Safety and Training: Building Best Practices

    Any chemical in daily use brings its own set of safety points. I’ve noticed that new lab members pick up protocols fastest when materials behave predictably. 4-Bromopyridine-2-Carboxamide presents low volatility, and its dust tends not to linger in the air compared to more finely powdered alternatives. This characteristic keeps airborne exposure risks down—a real benefit in tight lab spaces. Personal protective equipment like gloves and safety glasses remain the main line of defense, but users rarely run into acute, unexpected hazards from spills or splashes.

    Training new staff becomes smoother as a result. Experienced operators can highlight key storage guidelines, and because the compound doesn’t release strong odors or vapors, lab air stays cleaner. For institutions where health and safety oversight carries extra weight, stocking less volatile, more stable solids brings welcome reassurance.

    Driving Innovation With Smart Building Blocks

    For years, the focus in synthetic chemistry bounced between cutting costs and maximizing yield. Working with 4-Bromopyridine-2-Carboxamide usually ticks both boxes. Research groups can trust it to push reactions forward without demanding excessive catalysts or solvents. The compound’s unique combination of bromine and carboxamide often lets thinkers break away from old reaction patterns, taking risks on creative approaches that ultimately lead to the next big discovery.

    Innovation depends on tools that perform without drama. Using this molecule as a foundation, teams blend the rigorous standards of reproducibility with the freedom to try new functionalizations. I’ve seen it anchor projects from prototype drug analogues to targeted sensor components—the adaptability here cannot be overstated.

    Navigating Supply Chains and Economic Pressures

    No one wants to chase down backordered reagents while deadlines loom. In the current global supply climate, reliable access to chemical intermediates makes or breaks project timelines. Labs relying on 4-Bromopyridine-2-Carboxamide usually find a more robust supply chain than those entrenched in custom-made or niche intermediates. Established suppliers keep stock at the ready, which smooths out procurement headaches.

    Economic pressures have squeezed R&D budgets in recent years, but this compound generally remains accessible, even as other building blocks fluctuate in cost. The ability to purchase what’s needed, in bulk or small quantities, helps keep both costs and inventory in check. My experience has been that predictable pricing and on-time delivery help chemistry teams keep their promises on project milestones.

    Collaborative Gains in Multidisciplinary Research

    New medicines, diagnostic tools, and advanced materials don’t come together in a vacuum. They depend on seamless communication between teams of chemists, biologists, and engineers. A compound that sits at the intersection of useful and accessible fuels these collaborations. I’ve been in meetings where medicinal chemists puzzle out molecular structure-activity relationships while process chemists sketch routes for scale-up—4-Bromopyridine-2-Carboxamide often fits as a point of connection.

    In academic environments, its solid safety record, manageable handling, and broad synthetic applications open up creative educational projects. Years ago, I mentored undergraduates running their first coupling reactions, and having a forgiving, resilient compound on the bench let students focus on honing technique, not troubleshooting decomposition.

    Outlook and Path Forward

    As research moves toward ever more complex chemical architectures, the need for robust, adaptable intermediates will only sharpen. 4-Bromopyridine-2-Carboxamide positions itself as a cornerstone for both established and emerging chemical research. It speeds up cycles of hypothesis, testing, and iteration that push the field forward. My own work with this compound has saved both time and hassle—advantages that ripple out across full teams or entire research programs.

    Sustained support from trusted suppliers, clear documentation, and ongoing investments in safety and green chemistry practices only add to its appeal. In a world where demands for efficiency, safety, and sustainability often pull in competing directions, it grants a rare place of balance. Research groups that choose their building blocks wisely unlock more paths to scientific progress, and 4-Bromopyridine-2-Carboxamide consistently delivers on that promise.

    Final Thoughts on Practical Utility

    Every field faces buzzword fatigue, but real impact shows up in consistent results and streamlined operations. This compound checks those boxes time and again. Whether advancing medicinal chemistry, building new materials, or training the next wave of scientists, it represents the sort of advancement that matters—one that lets minds stay focused on solving the world’s next big challenges.