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8-Bromo-2H-1-Benzopyran-2-One

    • Product Name 8-Bromo-2H-1-Benzopyran-2-One
    • Alias 8-Bromocoumarin
    • Einecs 207-750-7
    • 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

    677699

    Product Name 8-Bromo-2H-1-Benzopyran-2-One
    Cas Number 6153-76-2
    Molecular Formula C9H5BrO2
    Molecular Weight 225.04
    Appearance Light yellow to brown powder
    Melting Point 177-182°C
    Purity Typically >98%
    Solubility Soluble in organic solvents (e.g., DMSO, ethanol)
    Synonyms 8-Bromocoumarin
    Smiles Brc1ccc2c(c1)oc(=O)cc2
    Inchi InChI=1S/C9H5BrO2/c10-6-3-1-2-5-4-7(11)12-9(5)8(6)11
    Storage Conditions Store at room temperature, away from light and moisture

    As an accredited 8-Bromo-2H-1-Benzopyran-2-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    More Introduction

    Meet 8-Bromo-2H-1-Benzopyran-2-One: Redefining Lab Tools

    Fresh approaches in research depend on standout building blocks. 8-Bromo-2H-1-Benzopyran-2-One has worked its way into chemists’ routines for a reason. It’s not just another chemical; people use it because it gets results you can trust. I still remember the first time I got my hands on a batch—white to off-white powder, like most laboratory standards, but with a real edge in reactivity where it counts. The moment you test the structure, there’s no mistaking the precision of that bromo group on the benzopyran core.

    Model: Some suppliers will list it under a straightforward numerical identifier, but ask anyone who works in medicinal chemistry or heterocyclic chemistry—this compound means business. The official IUPAC name is 8-bromo-2H-1-benzopyran-2-one, and the backbone structure lines up with some of the more creative pharmaceutical leads I’ve seen. The molecular formula clocks in at C9H5BrO2, giving it a comforting weight without making it unwieldy for benchwork.

    8-Bromo-2H-1-Benzopyran-2-One stands out from generic coumarin derivatives because the bromine atom is precisely at the 8-position. That shift creates more than just a detection handle for synthetic chemists. In medicinal chemistry, tweaking the halogen can alter a molecule’s activity, and every pro looks for that extra angle. Those who work with enzyme assays already know that subtle differences in electron distribution can change a lead compound’s selectivity toward enzymes and proteins. This isn’t just theory—I’ve seen collaborators leverage this particular molecule in exploratory fluorescence studies and even as a key halogenated intermediate for more advanced coumarin-based drugs.

    The specs say a lot about the quality, but you have to appreciate the simplicity that comes from purity upwards of 98%. Chromatography barely sweats it, and a dry, properly stored sample holds up under routine conditions. Anyone who runs multi-step synthesis cycles starts to appreciate these practical details. There’s nothing more frustrating than a batch that decomposes before you’ve even finished your route. This compound gives peace of mind—the crystalline structure resists moisture creep and gives clean spots in TLC.

    Real Advantages in Research and Production

    With 8-Bromo-2H-1-Benzopyran-2-One, you get more than a basic research material. Chemists who pivot between small-scale trial runs and scaled batch production see the difference. The high melting point works in the favor of anyone who needs a compound that keeps its structure under mild heating. In my own runs, I’ve had this hold steady through all the prep steps for downstream Suzuki or Heck couplings, with minimal byproducts. In the industry, wasted side products mean lost time and tighter margins, so companies circle back to this intermediate again and again.

    As for applications, lab teams lean on the versatility. Medicinal chemists reach for it while exploring novel anticoagulant scaffolds, as the benzopyran framework already sets the stage for biological testing. I’ve seen some biomed groups dabbling in imaging agents—particularly when fluorescence characteristics are needed—and this bromo-coumarin, with its unique halogen, opens doors for structural modifications. In academic settings, folks love the predictability when it comes to cyclization reactions, and journals echo this, referencing unique routes enabled by this exact template.

    Bench chemists spot the value in halogenated compounds again and again. It boils down to functional group compatibility and reactivity: 8-bromo on a benzopyran body lets you click together a robust family of derivatives without knocking out your budget on more exotic starting materials. The cost-effective factor always comes into reviews, especially in grant-driven research where every purchase gets scrutinized. I’ve discussed this with PIs who—like me—prefer choices that offer both straightforward handling and high scientific output.

    What Sets It Apart?

    Side-by-side with the parent coumarin molecule, the 8-bromo version isn’t just a one-note variant. The shift in electron density marks a clear distinction. Take standard coumarins: plenty of fluorescence, sure, but reactivity sometimes falls short when you attempt direct halogenation late in synthetic pathways. Here, you get the halogen already installed, saving multiple synthetic steps. Early introduction of bromine means less exposure for sensitive nuclei and better overall reliability in downstream transformations.

    Every compound brings strengths and weaknesses. With some analogues, the reactivity is too wild for practical applications; with others, the biological profile misses the mark. 8-Bromo-2H-1-Benzopyran-2-One wins points by threading that needle—the bromine brings enough heft to affect pharmacological activity while still keeping the synthetic window wide open for derivatization. I’ve seen postdocs troubleshoot recalcitrant targets with this compound, using its scaffolding properties to bridge gaps that other building blocks leave open.

    What keeps users loyal to this compound is the clear difference in downstream yields and spectrum profiles. Comparing to other brominated aromatics, this structure carries the signature resonance stabilization, so reactions push through smoothly. The crystalline, robust sample holds up under analyte characterization; NMR and mass spec analysts get sharp, predictable results, reducing troubleshooting time. Teaching labs that invest in undergraduate synthesis modules stick with this for its reliable response in student hands. It’s practical, not just theoretical.

    Reliable Sources Mean Better Outcomes

    Questions about purity or origin always matter in research settings. Any synthetic chemist will tell you a trusted supplier with batch traceability translates to safer, reproducible results. In my own work, I lean into supply chains that practice strict documentation, never cutting corners on storage or transportation. This builds confidence in every subsequent reaction step, maintaining the high standards expected for both academic papers and industrial research.

    Every now and then, someone brings up encountering off-color batches or shipments affected by environmental humidity. These moments underscore why built-in resilience is vital for such materials. Labs with limited environmental controls have come back to report that this substance, with its solid-state integrity, shrugs off most minor handling challenges. That’s something only a few alternatives manage, and it matters in large institutions as well as small startup environments.

    Shaping the Future for Medicinal and Synthetic Fields

    The story of 8-Bromo-2H-1-Benzopyran-2-One goes beyond short-term demand. Drug discovery leans on libraries of fluorophores and enzyme inhibitors, both fields where this molecule holds value. Screening campaigns for bacterial or fungal inhibitors take advantage of the way brominated scaffolds can unlock new binding pockets. Synthetic biologists tune properties for gene expression systems, sometimes starting with exactly this structure. It’s more than a piece of a puzzle; it can spark entire research trajectories.

    I’ve mentored students stepping into their first coumarin derivatization projects, and they quickly notice how this starting point offers options for both substitutions and cycloadditions. They get to circumvent some of the headaches of direct halogenation routes and appreciate how yields improve with fewer side reactions. Every mid-career scientist recognizes the time savings, adding new derivatives to the catalog without running into licensing headaches or convoluted regulatory restrictions.

    Of course, the solvent compatibility checks off every box: dissolves cleanly in commonly used organic solvents, so stock solutions prepare fast and reproducibly. This helps when pursuing high-throughput combinatorial synthesis campaigns. Screening hundreds of analogues isn’t a pipe dream—it becomes a regular workflow, with consistent results across plates. For anyone trying to bridge older methods with modern automation, these physical traits turn complexity into routine, daily progress.

    Analytical teams using HPLC and GC appreciate the compound for more than purity—the structure lends itself to clean separation, avoiding overlap with less well-behaved competitors. It’s a small thing at first glance, but saves hours on method development and validation.

    Facing Challenges and Finding Solutions

    Every chemical comes with risk if mishandled, so responsible stewardship sits at the center of safe lab work. I’ve seen less experienced teams skip fundamental PPE, only to suffer from unnecessary exposure. Fortunately, this compound’s solid form and moderate volatility minimize airborne hazards, but it pays to follow standard safety practice. Local safety data review avoids accidents, especially for new users.

    Waste management and environmental considerations tend to surface in conversations about halogenated aromatics. I encourage colleagues to keep updated on evolving guidelines for brominated waste. Many academic settings now run regular compliance checks. For small research outfits worried about sustainability, options such as solvent recycling and proper neutralization of waste streams help contain broader impacts. I’ve never regretted erring on the side of rigorous safety; good housekeeping makes for peaceful, productive labs.

    Sourcing also brings up ethical questions. Chemists and purchasing agents need to push for transparency—not just in technical sheets, but in labor and environmental claims from suppliers. You can’t overlook this in a world increasingly focused on responsible science. My peers tend to share supplier experiences, and a bad report spreads just as fast as a good one. Trust builds when companies invite audits or offer comprehensive documentation without resistance.

    Practical Strategies for Better Research Outcomes

    Teams can stretch the value of 8-Bromo-2H-1-Benzopyran-2-One by optimizing reaction conditions. Lowering temperatures in sensitive transformations improves selectivity and preserves fragile intermediates. If budgets allow, investing in more precise analytical instrumentation pays long-term dividends. The sharper you can monitor your reactions, the less likely you are to waste valuable reagents or miss subtle byproducts. I’ve found that cross-disciplinary input—borrowing ideas from analytical chemists and biologists—consistently leads to smarter experimental designs.

    Maintaining detailed lab notes makes a real difference. A simple spreadsheet log or digital LIMS platform guards against repeat mistakes and helps track batch-to-batch variability. Collaborative projects across multiple sites benefit from these records, as researchers can compare yield, purity, and performance data over time. Good habits stem from shared successes and honest reporting. I urge new hires to read up on case studies and documented synthetic failures, which can highlight the value of thoughtful compound selection.

    For startups and small enterprises, stretching supply budgets often means choosing compounds that serve more than one purpose. 8-Bromo-2H-1-Benzopyran-2-One fills that gap. Small teams get more out of each gram—testing, optimization, and validation can proceed without shopping for extra intermediates every cycle. From single-molecule projects to broader array syntheses, flexibility pays off.

    Looking Forward: Evolving with the Science

    As the pace of drug and materials discovery accelerates, having flexible, high-performance intermediates like 8-Bromo-2H-1-Benzopyran-2-One on the shelf makes all the difference. New analytics and automation solutions open doors for faster synthesis and expanded compound libraries. I’ve sat in on roundtables where research directors, regulatory experts, and vendors debate how to keep up with demand for ever-more-diverse building blocks. Consensus grows around investing in well-documented, robust molecules instead of chasing trendy but unproven options.

    Regulatory conversations matter, too. Access to safer, more predictable lab materials drives responsible growth. Every license approval or customs form benefits from standardized supply and honest, science-first communication between providers and researchers. The emergence of digital supply tracking and block-chain-backed documentation further reinforces the value chain. I urge others in my field not to overlook the basics: transparency, accuracy, and professional integrity matter as much as the molecule itself.

    Connecting Past, Present, and Future Research

    Long before automation and digital platforms defined research, bench chemists made incremental discoveries using tools like the benzopyran family. 8-Bromo-2H-1-Benzopyran-2-One keeps this tradition alive, blending time-tested reliability with modern expectations for purity, traceability, and adaptability. I’ve watched how a single compound, carefully chosen for its structure and reactivity, becomes the cornerstone of a project, setting a tone of collaboration and discovery that ripples outward.

    For those just starting out or seasoned investigators branching into new directions, investing time in understanding the subtle differences among available compounds always pays back. Watching teams transition from generic coumarin to its brominated cousin speaks to the importance of critical evaluation at every phase—planning, execution, and iteration.

    In all my years around lab benches old and new, the story repeats: dependable, versatile compounds shape the future of discovery. 8-Bromo-2H-1-Benzopyran-2-One stands as an example—fusing robust tradition and smart innovation, anchoring progress today while supporting the breakthroughs of tomorrow.