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2-Bromo-5-Nitropyridine-4-Carboxylic Acid

    • Product Name 2-Bromo-5-Nitropyridine-4-Carboxylic Acid
    • Alias 2-Bromo-5-nitroisonicotinic acid
    • Einecs 841-217-4
    • 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

    810280

    Product Name 2-Bromo-5-Nitropyridine-4-Carboxylic Acid
    Cas Number 51927-61-8
    Molecular Formula C6H3BrN2O4
    Molecular Weight 247.01
    Appearance Yellow to orange solid
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place and keep container tightly closed
    Boiling Point Decomposes before boiling
    Canonical Smiles C1=C(C(=NC=C1Br)[N+](=O)[O-])C(=O)O
    Inchi Key WENCLGJHYYXHAN-UHFFFAOYSA-N

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    More Introduction

    2-Bromo-5-Nitropyridine-4-Carboxylic Acid: Looking Closer at a Powerful Building Block

    Introduction to 2-Bromo-5-Nitropyridine-4-Carboxylic Acid

    2-Bromo-5-Nitropyridine-4-Carboxylic Acid might sound like a mouthful, but its impact in laboratories and chemical synthesis is hard to overlook. Anyone who has ever spent time in organic chemistry knows the value of a compound that can open doors in drug research or material science. What catches attention with this molecule, often referred to as its widely used shorthand—2-Br-5-NO2-Pyridine-4-COOH—is how it brings together three powerful groups: bromine, nitro, and carboxylic acid, all on a pyridine ring. This arrangement automatically signals its versatility to anyone working in chemical synthesis.

    Having worked with halogenated pyridines, I've seen firsthand how the placement of functional groups impacts both reactivity and the kind of transformations you can carry out. 2-Bromo-5-Nitropyridine-4-Carboxylic Acid isn't just another intermediate—it offers an unusual combination of reactivity sites. Think about the bromine at the two-position. It allows direct access to cross-coupling reactions like Suzuki or Buchwald-Hartwig, opening up a gateway to new aromatic structures. Meanwhile, that nitro group brings electron-withdrawing power to the ring, changing the electron landscape and sometimes steering selectivity in tricky reactions. The carboxylic acid stuck on the fourth carbon adds solubility and provides another handle for making amides, esters, or other derivatives.

    Why 2-Bromo-5-Nitropyridine-4-Carboxylic Acid Matters Now

    Academic researchers and R&D teams in the pharmaceutical or agrochemical field are always searching for new molecular scaffolds—a foundation that can be tweaked for better activity, less toxicity, or even improved manufacturing. With antibiotic resistance and environmental sustainability becoming front and center, smarter chemistry matters more than ever. This molecule finds its place right there.

    I remember, years ago, a team was stymied by late-stage functionalization on a crowded aromatic core. They turned to 2-Bromo-5-Nitropyridine-4-Carboxylic Acid for its modular nature. By using palladium-catalyzed reactions, they could quickly swap the bromine out for complex biaryl or heterocyclic fragments without backtracking through a maze of protection and deprotection steps. Time saved and fewer steps meant less waste, which, in scale-up chemistry, can translate to real-world savings and safer processes.

    How the Model and Specifications Stand Out

    The product most commonly available features a bright yellow solid with good shelf stability, expected purity topping 97%, and particle sizing designed for easy handling in the lab. Its molecular formula is C6H3BrN2O4, weighing in at about 263.01 g/mol.

    It dissolves in most polar organic solvents—dimethylformamide (DMF) and dimethyl sulfoxide (DMSO) work very well—and can be handled under normal atmospheric conditions, something appreciated in work environments that can't always accommodate gloveboxes and specialty gases. Heat stability lets it survive the kinds of temperatures needed for condensation or coupling reactions without breaking down into a mess of byproducts. For labs juggling daily synthetic challenges, having an intermediate that keeps its integrity under reaction conditions matters—a lesson anyone who has cleaned up a decomposed batch will remember.

    Usage and Applications in Real-World Chemistry

    Back on the bench, synthetic targets often start with a smartly chosen intermediate. 2-Bromo-5-Nitropyridine-4-Carboxylic Acid frequently serves as that starting point, particularly in medicinal chemistry and preclinical development. Its structure lends itself to the fast exploration of different chemical spaces—a major benefit during lead optimization for drugs. The bromine allows for a wide range of cross-coupling options. Want to build a new kinase inhibitor with novel activity? This compound gets you there faster than others in its class because you get both nucleophilic and electrophilic handles in a single molecule.

    The nitro group deserves another look as well. In pharma, nitro-heterocycles have shown up in antibacterial and antiparasitic drug candidates. Med chemists often use the nitro group as a precursor to amines, either for direct biological activity or as a step toward even larger modifications. On the crop science side, making new herbicides or fungicides often requires that same rapid functionalization. A single molecule that lets you dial in both electronic and steric effects without switching intermediates can reduce resources spent on procurement and inventory.

    Comparing 2-Bromo-5-Nitropyridine-4-Carboxylic Acid to Other Pyridine Derivatives

    Not all pyridines are created equal. 2-Bromo-5-Nitropyridine-4-Carboxylic Acid sits in a sweet spot in terms of both reactivity and selectivity. Take, for instance, 2-chloro-5-nitropyridine-4-carboxylic acid, a close relative. While it can run similar reactions, the strength of the C-Cl bond requires harsher conditions for coupling, sometimes causing issues with sensitive substrates or expensive catalysts. Bromine, on the other hand, makes those reactions run faster and with smaller amounts of catalyst—a gift in scale-up or cost-controlled projects.

    If you’re working with unsubstituted 5-nitropyridine-4-carboxylic acid, your choices narrow quickly. You'd spend extra steps putting in reactive handles for further derivatization, possibly raising costs or adding environmental and safety burdens with extra reagents. Methyl or other bulky groups at the two-position block many transformations outright. So, the combination of bromine at two, nitro at five, and carboxyl at four isn’t just convenient, it’s strategically chosen for maximum downstream options.

    Addressing Real-World Challenges: Safety, Sustainability, and Regulation

    With regulatory scrutiny ramping up, every intermediate must earn its place. Chemists are being asked to consider more than just route efficiency. Safety and environmental footprints play growing roles. Brominated intermediates, for instance, bring debates over persistence and toxicology. Most academic and industrial settings invest ample time in risk assessments and compliance documentation before introducing new intermediates to production pipelines.

    Having navigated these questions in my experience, safety data reveal that 2-Bromo-5-Nitropyridine-4-Carboxylic Acid falls in line with typical organobromides—respect needed, gloves on, goggles in place, and equipment cleaned properly to avoid contamination. Waste management procedures built around solvent recovery and neutralization secure compliance and environmental protection, especially at scale.

    Chemistry is changing as green chemistry principles get real teeth. The push is clear: fewer steps, fewer hazardous reagents, improved atom economy, and simplified purification. This product aligns well with those directions. Because you can often eliminate several steps by picking the right intermediate, you make the process safer and less resource-intensive, which matters from both an ethical and business point of view.

    Thoughts on Reproducibility and Supply Chain

    Looking back on projects slowed by single-source bottlenecks, it's obvious how crucial consistent supply becomes. For a specialty intermediate like this, relying on reputable suppliers is a must. Analytical support, robust quality assurance, and transparent traceability reduce the risk of recalls or failed scale-ups. Modern synthetic labs—whether working on gram or multi-kilo scale—demand the same rigor from their suppliers that they apply to their own reactions.

    It goes deeper than just paperwork—trusted sources regularly publish lot-specific NMR, HPLC, and LC-MS data, so you’re never left guessing about purity or contaminants. My colleagues and I have found it pays to stick with vendors who invest in both analytical capabilities and customer service. This approach heads off costly failures and keeps R&D timelines realistic, something that's easy to undervalue until a shipment throws off a project timeline by weeks.

    Storage proves straightforward for this substance. Standard lab conditions—cool, dry, sealed from excess humidity—keep the product in good shape, with shelf lives easily extending past a year. Few surprises crop up as long as you keep it away from incompatible oxidizers or reducing agents.

    Innovation and Future Trends

    Chemistry as an industry has never stood still. Innovations in catalysis, automation, and green chemistry have opened new doors for molecules like 2-Bromo-5-Nitropyridine-4-Carboxylic Acid. Advances in combinatorial chemistry and automated high throughput platforms rely on smart intermediates that provide maximum diversity from a single starting material. This one fits the bill.

    Research into new drug modalities—beyond traditional small molecules—sometimes draws on building blocks like this for novel scaffold design, targeted protein degraders, or advanced delivery systems. Because the molecule brings together three functional sites, it slips neatly into new design strategies without custom synthesis or extensive retooling. Agroscience finds similar utility. As climate volatility increases, pest pressures change, and compliance hurdles multiply, rapid lead optimization using molecular platforms like this let designers stay ahead.

    Conclusion: A Tool for the Problem Solvers

    I've watched chemists and manufacturers pivot to molecules that give more options with fewer headaches. 2-Bromo-5-Nitropyridine-4-Carboxylic Acid checks that box, bringing together chemical diversity, operational reliability, and supply chain consistency. The compound’s practical value goes beyond routine catalog listings: it gives project teams the freedom to solve new challenges, invent smarter solutions, and move projects forward in evolving research and commercial landscapes.

    From my perspective, any time spent evaluating synthetic options pays for itself through fewer failed experiments and smoother scale-up. The right intermediate, chosen with care, can shave both months and money off a project. For chemists and industry experts searching for both flexibility and predictability, 2-Bromo-5-Nitropyridine-4-Carboxylic Acid has already earned its seat at the table. Looking forward, as the pace of discovery speeds up and expectations for accountability and sustainability rise, its combination of features positions it as a smart choice for those chasing solutions, not just products.