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5-Bromo-4-Chloro-1H-Indazole

    • Product Name 5-Bromo-4-Chloro-1H-Indazole
    • Alias 5-Bromo-4-chloroindazole
    • Einecs 629-714-9
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    481354

    Product Name 5-Bromo-4-Chloro-1H-Indazole
    Molecular Formula C7H4BrClN2
    Molecular Weight 231.48 g/mol
    Cas Number 885272-32-6
    Appearance Off-white to light yellow solid
    Melting Point 187-191°C
    Solubility Slightly soluble in DMSO and DMF
    Purity Typically >97%
    Smiles Clc1c(Br)cc2[nH]ncc2c1
    Inchi InChI=1S/C7H4BrClN2/c8-5-3-6-7(4-1-2-10-11-6)9/h1-4H,(H,10,11)
    Storage Condition Store at room temperature, protected from light
    Synonyms 4-Chloro-5-bromo-1H-indazole

    As an accredited 5-Bromo-4-Chloro-1H-Indazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 5-Bromo-4-Chloro-1H-Indazole

    Applications of 5-Bromo-4-Chloro-1H-Indazole in Industrial Manufacturing

    As a specialized manufacturer of 5-Bromo-4-Chloro-1H-Indazole, we support multiple downstream industries with reliable supply, batch consistency, and technical documentation aimed at high-value industrial synthesis. Our expertise ensures each application scenario meets specific chemical, regulatory, and process integration requirements in real-world production environments.

    1. Pharmaceutical Intermediate for Kinase Inhibitor Development

    5-Bromo-4-Chloro-1H-Indazole functions as a critical scaffold in the synthesis of kinase inhibitor APIs, particularly compounds targeting oncological and autoimmune indications. Downstream pharmaceutical companies use this raw material in the early-stage build-up of heterocyclic systems integral to medicinal chemistry routes. We provide tailored documentation and purity grades to support cGMP requirements, enabling seamless batch release in regulated drug substance production. Our technical support assists with impurity profiling, solvent compatibility, and scale-up consultation to help customers pass regulatory audits.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF guidelines for intermediates
    • EU EudraLex Volume 4 GMP Annexes
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 0.2–1.4 molar equivalents relative to the downstream core structure, adjusted per medicinal chemistry route and desired substitution pattern.

    Downstream process integration

    • Introduced during the indazole-based coupling or reductive amination stage of multi-step API synthesis.
    • Processed in controlled reaction vessels with in-process monitoring for purity and byproduct management.

    Final product types

    • Small molecule kinase inhibitors (oncology, immunology)
    • Investigational new drug (IND) candidates
    • Branded and generic pharmaceutical APIs containing indazole moieties

    2. Agrochemical Intermediate for Selective Herbicide Synthesis

    This indazole compound serves as a foundational intermediate in the synthesis of new-generation selective herbicides, supporting research and commercial scale-up activities in crop protection. Downstream formulators use it to construct indazole-derived actives, which show enhanced selectivity for weed species and resistance to environmental degradation. We ensure raw material traceability, provide analytical certificates aligning with ISO and OECD requirements, and offer technical guidance on impurity control during downstream reactions for high-yield actives.

    Industry compliance standards

    • ISO 9001:2015 for chemical manufacturing
    • FAO/WHO Specifications for Plant Protection Products
    • OECD Guidelines for the Testing of Chemicals
    • REACH Regulation (EC) No 1907/2006 for chemical registration

    Typical usage ratio

    • 0.4–0.8 molar equivalents based on the engineered indazole core of target active ingredient, adapted to specific synthetic route and final herbicide structure.

    Downstream process integration

    • Reacted in nucleophilic substitution or cyclization steps following the initial assembly of the core molecule.
    • Integrated with chlorination or bromo-functionalization stages using automated dosing equipment.

    Final product types

    • Pre- and post-emergence herbicides for cereal and broadleaf crops
    • Technical concentrates for formulation plants
    • Herbicide actives formulated in suspension concentrates and water-dispersible granules

    3. Building Block for Advanced Electronic & OLED Materials

    In the electronics sector, our indazole derivative offers electronic properties and molecular rigidity prized for organic light-emitting diode (OLED) and small-molecule semiconductor synthesis. Specialty materials manufacturers incorporate this intermediate during the assembly of complex, conjugated structures that affect luminosity, charge-carrier mobility, and device stability. We guarantee batch traceability, provide impurity mapping for electronic purity needs, and supply technical packs fitting ISO and IEC standards for materials entering consumer electronics value chains.

    Industry compliance standards

    • ISO 9001:2015 for quality management in specialty chemicals
    • IEC 62679 for display panel components
    • RoHS Directive 2011/65/EU for hazardous substance control
    • Supplier assessment as per JEITA guidelines

    Typical usage ratio

    • 1:1 stoichiometry in cross-coupling or Suzuki-Miyaura reactions, customized to functional group compatibility and electronic property targets.

    Downstream process integration

    • Used as a precursor for indazole-based light-emitting and electron-transport layer compounds.
    • Fed into automated synthesis lines for scale-up pilot or production batches under inert environments.

    Final product types

    • OLED emitter materials and host matrices for display and lighting panels
    • Thin film transistors and small-molecule semiconductors
    • Electronic chemical precursors for high-value device components

    4. Intermediate for Veterinary Drug Substance Synthesis

    Veterinary drug manufacturers select this indazole compound for the development of antiparasitics and anti-inflammatory actives for farm and companion animals. We deliver volumes suitable for pilot and commercial scale, backed by VICH-compliant documentation. Our technical team assists with solvent and impurity compatibility necessary for high-purity veterinary APIs. Strict adherence to animal health regulations and customer audit requirements promote safety and reliability in feed and injectable products.

    Industry compliance standards

    • VICH GL guidelines for veterinary active substances
    • GVP (Good Veterinary Practice) compliance for intermediates
    • US FDA CVM (Center for Veterinary Medicine) specification protocols
    • ISO 9001:2015 for animal drug supply chains

    Typical usage ratio

    • 0.3–1.0 molar equivalents, selected based on target API synthesis pathway and required animal health specification.

    Downstream process integration

    • Charged into key condensation or alkylation steps in the upstream synthesis of veterinary APIs.
    • Controlled addition at low temperatures to manage sensitive functional groups and avoid decomposition.

    Final product types

    • Veterinary antiparasitic APIs
    • Anti-inflammatory actives for animal health
    • Medicated premixes for commercial animal feeds
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    More Introduction

    Introducing 5-Bromo-4-Chloro-1H-Indazole: A Key Indazole Compound for Modern Research and Synthesis

    Every seasoned chemist knows the indazole skeleton opens doors to a surprising range of applications, from drug discovery to advanced material science. Whether in a university lab or a pharmaceutical startup, researchers keep coming back to trusted intermediates that show reliability, purity, and performance. Among them, 5-Bromo-4-Chloro-1H-Indazole stands out. If you’ve ever struggled with limited compound libraries or cumbersome synthesis routes, this molecule marks a turning point by anchoring your plans with its unique characteristics.

    Molecular Structure and Model Insights

    The core structure involves a fused benzene and pyrazole ring, with precise substitutions at the 5 and 4 positions: bromine and chlorine, respectively. The molecular formula reflects this, and the placement of halogens changes how the molecule reacts, binds, and serves as a building block. Choices like these make a difference. Sometimes, the way a molecule fits into a reaction provides the competitive edge in medicinal chemistry or advanced organic synthesis. The physical specifications usually translate into high stability, clear crystallinity, and easy handling, letting researchers focus less on purification headaches and more on breakthrough ideas.

    Applications that Rely on Targeted Precision

    Chemists often reach for 5-Bromo-4-Chloro-1H-Indazole when mapping out multi-step syntheses for heterocyclic scaffolds. Experienced professionals know the challenge of finding suitable partners for Suzuki, Buchwald-Hartwig, or nucleophilic substitution reactions. This compound’s bromine and chlorine attachments unlock activity at both positions, acting as ready handles for cross-coupling, making it pivotal for introducing complexity into molecules without laborious protection and deprotection steps. In drug discovery programs, indazole derivatives frequently form the backbone of kinase inhibitors, anti-inflammatory agents, and antimicrobial candidates. The 5-bromo and 4-chloro pattern doesn’t just add variety — it helps tune target affinity and metabolic resistance, which can shift a project from stalled to promising.

    If you regularly work in medicinal chemistry, you'll recognize the nimbleness this molecule introduces into SAR studies. Modifying just one position with high fidelity lets research teams deliver more options to the biology group, which matters when lead candidates start narrowing. Outside pharma, this indazole finds its way into agrochemical development, functional dyes, OLED materials, and specialty polymers. The spectrum of opportunities reflects broad industry confidence in the reliability of such halogenated indazoles.

    Differences from Other Indazole Derivatives

    For any lab, choosing between variants like 5-bromo-1H-indazole, 4-chloro-1H-indazole, or their unsubstituted counterpart means weighing chemical reactivity, stability, and cost. What sets 5-Bromo-4-Chloro-1H-Indazole apart isn’t just the dual halogen tagging. The arrangement at both 5 and 4 means you can selectively run downstream substitutions, like arylation, amination, or metal-catalyzed reactions, with greater control over side reactions. In my own past work on kinase target projects, single-halogen indazoles sometimes suffered from sluggish coupling and unpredictable byproducts. Introducing both bromine and chlorine improved outcomes, with less troubleshooting and cleaner NMRs, which any synthetic chemist can appreciate.

    Researchers working with similar compounds quickly learn the importance of position-specific reactivity. A 5-bromo substitution influences electron withdrawal at the nearby nitrogen, but pairing it with a 4-chloro group adjusts the electron density even further. While no substitution pattern is a solution for every project, this particular fingerprint opens channels to finish more elaborate substitution plans with fewer steps. Chemically, that translates into reduced time, fewer resources spent on failed reactions, and an edge in competitive grant applications or tight commercial timelines.

    Quality, Handling, and Consistency

    High standards in chemical supply can’t be taken lightly. I recall running into inconsistencies with off-brand intermediates during a medicinal chemistry campaign: minor impurities, slight changes in melting point, problems with solubility. After switching to supplies of 5-Bromo-4-Chloro-1H-Indazole from reputable distributors who prioritized purity, batch-to-batch reliability improved, and downstream yields benefited. Most labs today source this compound as a white to off-white crystalline solid, commonly sold at high purity standards exceeding 98%. For bench chemists, this means less time invested in recrystallization or tedious chromatography before scaling up reactions.

    Storing the solid at room temperature in tightly capped bottles, away from moisture and light, extends shelf life and keeps degradation at bay. The stability of 5-Bromo-4-Chloro-1H-Indazole means researchers can plan long-term projects without stressing over sudden loss of reactivity due to oxygenation or photolysis. Its handling profile offers peace of mind compared with more labile or sensitive indazole analogs.

    Benefits of Consistent Specifications

    Sticking to strict batch specifications helps avoid inconsistencies that rob labs of precious time. Contractors, graduate students, and full-time researchers all share stories of weeks lost troubleshooting reactions that stalled due to marginal reagent quality. By setting clear parameters for melting point, appearance, and residual solvent content, suppliers support solid reproducibility. For those aiming to publish data, submit supporting information, or satisfy regulatory filings, that kind of documentation makes the difference between a pass and endless rounds of review.

    Rigorous specifications aren’t about bureaucracy. They help teams turn out reliable work and build trust in joint ventures, academic-industry collaborations, and patent applications. My own short stint managing a shared instrumentation facility taught me that even the best synthesis or screening campaign gets derailed by poor documentation or imprecise starting materials. Standardized supply chains and clear labels on key intermediates like 5-Bromo-4-Chloro-1H-Indazole empower everyone from undergraduates to principal investigators.

    Responsible Usage and Safety Mindset

    Anyone who has mixed powders or run reflux reactions knows lab safety can’t take a back seat. Indazole derivatives with halogens, including 5-Bromo-4-Chloro-1H-Indazole, require sensible handling. Common PPE — gloves, goggles, lab coats — sets the baseline. Most labs use chemical hoods, not just for compliance but also for sheer practicality. This compound, while not notorious for extreme hazards, still deserves respect. No one wants to deal with minor irritations, unexpected inhalation risks, or spilled material during weighing.

    Every responsible lab maintains access to up-to-date safety data. Proper waste labeling, segregated halogenated organic waste streams, and spill kits shouldn’t be seen as chores — they’re simply the fabric of good research culture. Over the years, I’ve seen colleagues avoid incidents not by over-preparing but by staying mindful and organized on the bench. Following written protocols and consulting safety data keeps labs productive and shields them from costly mishaps.

    Ensuring Scientific Integrity with Trustworthy Compounds

    Experienced research teams look beyond label claims. They run their own TLC checks, NMRs, and purity tests. The best suppliers of 5-Bromo-4-Chloro-1H-Indazole don’t shy from third-party verification, and neither should buying consortia or grant-funded groups. Backed by certificates of analysis, these products let labs publish confidently, knowing their SAR, yield, and analytical data won’t be questioned on the grounds of reagent impurity. That transparency strengthens results and reduces headaches downstream.

    Younger researchers sometimes overlook these steps, eager to jump straight into chemistry. Long-term, habits built around double-checking sources and specs save not just time but also research reputations. The value of accurate starting material shows up during review processes or patent filings, where ambiguous identities or characterization gaps can halt progress. For 5-Bromo-4-Chloro-1H-Indazole, detailed documentation and reliable supplier history shift the odds toward smoother projects and more meaningful discoveries.

    Driving Innovation with Strategic Building Blocks

    Modern research lives on speed and adaptability. Flexible intermediates like 5-Bromo-4-Chloro-1H-Indazole allow teams to pivot quickly between different synthetic strategies. In my experience, the halogen pattern supports advanced cross-coupling, direct amination, or even late-stage diversification after main coupling steps finish up. Other indazole variants lock researchers into limited options, sometimes leading to dead ends or tedious protection group gymnastics.

    This compound doesn’t just make synthetic chemistry easier — it encourages more creative routes, faster library construction, and more nuanced SAR investigation. Whether you're scaling a synthesis or setting up milligram reactions, having stable, well-characterized building blocks at hand sharpens focus. Labs can experiment further, knowing the critical piece won’t fail due to instability or unknown impurities.

    Comparative Edge over Common Alternatives

    Not all indazole derivatives perform equally across applications. I’ve tried 5-bromo-indazoles that lag in cross-coupling, or 4-chloro-analogues that resist nucleophilic displacement. The 5-bromo-4-chloro backbone lets chemists coordinate more efficient multi-step development by providing two separate sites for orthogonal substitution or sequential functionalization, reducing the iterative cycle of protection and deprotection.

    In process chemistry, this means fewer operations: less chromatography, minimal intermediate purification, and more robust scalable routes. Feedback from colleagues in process R&D confirms that projects using this dual-substituted indazole often finish with higher throughput, higher isolated yields, and lower cost per gram produced. Those factors add up, especially in early-stage drug programs or commercial pilot runs, where chemistry bottlenecks can erode timelines.

    Stepping Up to Tomorrow’s Demands

    The demand for custom indazoles keeps growing in pharma, electronics, agrochemical research, and functional materials. As structure-activity relationships become sharper and more data-driven, starting materials can’t fall short on quality or versatility. Working with dependable intermediates like 5-Bromo-4-Chloro-1H-Indazole supports everything from fast analog preparation to pilot scale reactions in process chemistry plants. It may look like just another bottle on the shelf, but for those deep in synthesis, it’s a linchpin for progress.

    Collaborative projects, whether between global companies or in multi-disciplinary academic groups, lean on standardized and reliable chemical inputs. As requirements for data integrity and reproducibility become more rigorous, materials like 5-Bromo-4-Chloro-1H-Indazole stand under brighter scrutiny. Experience shows that investing in well-validated intermediates pays off not just in technical outcomes, but in trust between partners. Credibility often starts at the molecular level, setting the tone for every result that follows.

    Final Thoughts for Modern Chemists

    Chemistry at the front lines of innovation depends on stable, thoroughly characterized intermediates that make experimental work less daunting and more productive. Every compound has a story, but compounds like 5-Bromo-4-Chloro-1H-Indazole become silent partners to research breakthroughs. Long-term experience teaches that reliable supply, clarity of specifications, and proven reactivity aren’t luxuries — they’re the difference between another failed run and a successful series of experiments.

    For seasoned professionals and those just starting out, treating intermediates with the respect they deserve ensures progress today and excellence tomorrow. Choosing wisely, investing in quality, and maintaining a culture of responsible handling keeps the doors open for better science. 5-Bromo-4-Chloro-1H-Indazole, with its combination of versatility, reliability, and adaptability, exemplifies the kind of building block that defines smart synthesis and drives discovery forward.