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2-Bromo-6-Chloropyrazine

    • Product Name 2-Bromo-6-Chloropyrazine
    • Alias 2-Bromo-6-chloropyrazine
    • Einecs 838-357-7
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    956537

    Chemical Name 2-Bromo-6-Chloropyrazine
    Molecular Formula C4H2BrClN2
    Molecular Weight 193.43 g/mol
    Cas Number 24171-42-8
    Appearance White to light yellow solid
    Melting Point 49-51°C
    Purity Typically ≥97%
    Synonyms 6-Chloro-2-bromopyrazine
    Smiles C1=CN=NC(=C1Cl)Br
    Inchi InChI=1S/C4H2BrClN2/c5-3-1-7-8-4(6)2-3/h1-2H
    Solubility Slightly soluble in common organic solvents
    Storage Conditions Store in a cool, dry place, away from light

    As an accredited 2-Bromo-6-Chloropyrazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 2-Bromo-6-Chloropyrazine

    Applications of 2-Bromo-6-Chloropyrazine in Industrial Manufacturing

    2-Bromo-6-Chloropyrazine functions as a critical building block in fine chemical processes and custom molecule synthesis. Its unique halogen arrangement supports advanced API intermediates, agrochemical development, and specialty material engineering. As a direct manufacturer, we support diverse downstream sectors with traceable, high-quality source materials tailored for regulated and large-scale production environments.

    1. Pharmaceutical Intermediate Synthesis (API Development)

    Major pharmaceutical companies utilize this compound as an intermediate in multi-step syntheses, especially in the preparation of oncology and antiviral drug precursors. The electron-withdrawing bromine and chlorine facilitate selective heterocycle functionalization, supporting robust cross-coupling and amination steps. Stringent raw material identity and purity controls ensure downstream compliance from pilot scale to full cGMP manufacturing.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Part 211 (FDA Drug Manufacturing)
    • USP/EP Residual Solvent and Elemental Impurity Guidelines
    • GMP audit documentation and batch traceability under ISO 9001:2015

    Typical usage ratio

    • Batchwise input at 1–10 mol% of target API molecular weight
    • Stoichiometry varies by specific synthetic route and coupling processes

    Downstream process integration

    • Direct use in Suzuki/Miyaura or Buchwald–Hartwig cross-coupling reactions
    • Foundation structure for heterocyclic core assembly (Stage 2–4 in multistep synthesis)
    • Feeding into parallel synthesis for analog screening
    • In-process control using HPLC and NMR for structural verification

    Final product types

    • Anticancer API precursors (e.g., kinase inhibitor backbones)
    • Antiviral nucleoside analog intermediates
    • CNS active heterocycle API candidates
    • High-purity research-scale pharmaceutical intermediates

    2. Crop Protection Active Ingredient Production

    Agricultural chemical manufacturers employ this material in the synthesis of active ingredients for herbicides and fungicides featuring pyrazine rings. The molecule’s dual-halogen profile supports selective acylation and thiolation, which are critical in achieving biological activity and field stability in crop protection agents. Adherence to global agrochemical manufacturing regulations, quality batch release, and impurity profiling supports sustainable production.

    Industry compliance standards

    • FAO/WHO Guidelines for Agricultural Pesticide Specifications
    • OECD Principles on Good Laboratory Practice
    • ISO 9001:2015 for production and batch release
    • REACH (EU Regulation No. 1907/2006) substance registration and evaluation

    Typical usage ratio

    • Feed ratios of 2–8% by weight relative to target protection agent synthesis batch size
    • Adjusted depending on chlorination and target molecule structural requirements

    Downstream process integration

    • Initial halogenated pyrazine coupling for creating bioactive backbones
    • Stepwise derivatization in pilot and commercial synthesis
    • Pre-formulation scale-up and impurity removal under strict QC
    • Integration into solvent or aqueous batch reactors

    Final product types

    • Selective herbicide intermediates
    • Broad-spectrum fungicide core structures
    • Chemistries for insect growth regulators
    • Active ingredients for formulated crop protection solutions

    3. Pharmaceutical Research and Development Libraries

    Contract research organizations (CROs) and pharmaceutical R&D centers use the compound in combinatorial chemistry for generating focused libraries of novel heterocyclic molecules. The distinctive dual-halogen substitution pattern enables rapid SAR (structure-activity relationship) exploration by allowing further substitution or coupling, benefiting high-throughput screening campaigns under regulated laboratory and intellectual property frameworks.

    Industry compliance standards

    • GLP (Good Laboratory Practice) compliance (OECD and FDA)
    • ISO 17025 for laboratory quality and analytical testing
    • Secure substance management under institution-specific chemical hygiene plans
    • Material transfer agreements (industry and CRO settings)

    Typical usage ratio

    • 0.5–5 mmol per split synthesizing sublibrary arm
    • Variable, optimized for resource-efficient parallel synthesis and diversity generation

    Downstream process integration

    • Foundation for parallel small-molecule library construction
    • Introduction point for cross-coupling and aromatic substitution reactions
    • LC/MS and NMR profiling for purity and identity assurance
    • Repurposing into novel lead compound generation for bioassay screening

    Final product types

    • Diversified heterocyclic screening libraries
    • Patentable small molecule templates
    • Analytical standards for pharmaceutical research
    • Candidate compounds for medicinal chemistry optimization

    4. Electronics and Specialty Materials Synthesis

    Electronics and advanced material manufacturers incorporate this halogenated pyrazine during functional material development, particularly in organic thin-film transistors and OLED emitters. The molecule promotes charge transport and stability due to the pyrazine core’s aromaticity and the halogen atoms’ impact on molecular orbitals. Stringent quality control ensures suitability for electronic-grade applications.

    Industry compliance standards

    • IEC 60747 (Semiconductor Device Standards)
    • IPC-A-610 (Electronic Assemblies Acceptability)
    • RoHS Directive 2011/65/EU for hazardous substances
    • ISO 14644 Cleanroom Standards

    Typical usage ratio

    • Used at 0.5–5 wt% in advanced organic material precursor blends
    • Exact proportion tailored per electronic property and final device requirements

    Downstream process integration

    • Condensation and substitution steps in electronic-grade intermediate synthesis
    • Mixing with aryl or alkynyl coupling partners for organic device layer fabrication
    • In-line purity assessment (GC, HPLC, residual metal analysis)
    • Transition to downstream thin-film coating or vapor deposition

    Final product types

    • Organic semiconductors
    • Thin-film transistor intermediates
    • OLED material precursor blends
    • Specialty polymers for electrical insulation
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    Certification & Compliance
    More Introduction

    Introducing 2-Bromo-6-Chloropyrazine: A Reliable Intermediate for Advanced Synthesis

    A Practical Chemistry Companion

    Bringing new compounds to life starts with reliable building blocks. In a landscape where every foundation matters, 2-Bromo-6-Chloropyrazine stands out as a versatile and dependable starting point for design in both research and industrial chemistry. With a unique configuration featuring both bromine and chlorine on a pyrazine core, this compound offers opportunities to take synthesis in diverse directions, especially valuable for fine chemicals and pharmaceutical development.

    Model and Chemical Features

    Carrying the molecular formula C4H2BrClN2 and a molecular weight of about 193.44 g/mol, this compound appears as an off-white crystalline powder. The structure brings together two reactive halogens, which makes selective substitution feasible. Researchers value this dual reactivity; they can tailor pathways for Suzuki-Miyaura couplings, nucleophilic aromatic substitutions, and heterocycle extension. The reliability of this model helps chemists reduce guesswork in multi-step procedures. Through direct experience in the lab, I've seen how dual halogenation expands the options for late-stage functionalization, so the chemist gets more freedom to react with confidence.

    Usage in Industry and Research

    2-Bromo-6-Chloropyrazine has earned its place as a dependable intermediate for many laboratory and plant-scale settings. Synthetic chemists often gravitate toward halogenated pyrazines for a good reason: these molecules serve as scaffolds for new candidate drugs, agrochemical agents, and specialty materials. Pyrazine rings show up in a wide range of applications, from therapeutic antivirals to performance polymers.

    This compound is especially useful when the synthesis calls for flexible yet accessible transformation points. In drug discovery, the bromine and chlorine groups let researchers introduce new functional groups without the extra steps that an unactivated or fully substituted ring would require. Compared to pyrazines with only a single halogen, this dual-substituted variant can streamline the process, cutting down on the number of reaction sequences and the time spent purifying intermediates.

    For agrochemical developers, working with a compound that offers distinct reactivity opens more room for creating focused libraries of candidates. This means that instead of making countless starting materials from scratch each season, teams can revisit and remix structures quickly. In material science, the reliability and reactivity pattern open up applications in electronic materials, for example, in organic semiconductors or as building blocks for ligands in coordination chemistry.

    Purity, Handling, and Bench Experience

    In my own work, using a highly pure sample of 2-Bromo-6-Chloropyrazine means fewer downstream headaches — fewer side reactions crop up, and chromatography doesn’t drag into endless hours. Consistency counts, especially when processes demand repeatable results, week after week. Typical purities for benchmarking synthesis hover above 97%, and slight deviations can affect yields or introduce unwelcome byproducts.

    Storing the powder in a cool, dry place shields it from hydrolysis and degradation. Laboratory routines, like weighing and transfer, tend to go smoothly given the compound’s crystalline, non-hygroscopic nature. Its modest odor and manageable volatility make it user-friendly compared to some other halogenated intermediates that release irritating vapors. Personal experience confirms that working with this compound doesn’t mean constant glove changes or elaborate fume-hood gymnastics.

    Differences from Other Pyrazine Compounds

    What distinguishes 2-Bromo-6-Chloropyrazine from single-halogenated or fully-substituted analogs is its blend of selectivity and adaptability. Single-chloro or single-bromo pyrazines may limit the ways in which a chemist can approach further functionalization. For instance, the bromine, being more reactive under many palladium-catalyzed conditions, invites smooth cross-coupling. Chlorine, less reactive but more durable, allows for stepwise reactions when needed. Multihalogenated variants can bring instability or complicate purification. Here, the balance between activation and selectivity can mean all the difference, particularly when tight budgets force careful planning.

    Over the years, colleagues and I have noticed that dual-halogenated compounds open up synthetic schemes that would otherwise require several extra steps. Less time retesting, less solvent waste, and fewer hazardous byproducts trickle out at the end of the workup, making this compound a favorite not only for ease but also for the environmental footprint. Compared to monohalogenated species, you’ll get better mileage out of 2-Bromo-6-Chloropyrazine in divergent or convergent syntheses, which in practical terms means faster go-to-market timelines for complex projects.

    Real-World Impact and Applications

    Outside of theoretical appeal, results in the real world matter most. In pharmaceutical R&D, the speed at which a modular intermediate like this leads to a library of analogs can set teams apart. Molecules built on halogen-rich cores typically display improved cell permeability, increased metabolic stability, or even patentability — essential factors in competitive innovation cycles. For anyone involved in process design or scale-up, the predictability of 2-Bromo-6-Chloropyrazine reactions helps mitigate surprises. A smooth route from gram to kilogram scale reduces material losses and improves documentation for regulatory filings.

    Academics often select this compound for research into ligand design or to probe fundamental reactivity trends. With two different halogens, undergraduate and graduate students can explore selectivity, substitution mechanisms, and catalyst behavior, all from a single, manageable substrate. Workshop sessions using this compound tend to foster lively discussion, as the side-by-side chemical possibilities show the importance of smart substrate choice.

    The food and flavor industry may also draw on the pyrazine scaffold, thanks to its recognizable aromatic backbones. While direct use in finished consumer products is less common with halogenated derivatives, intermediates like this shape the way new molecules are discovered and brought to shelf. Every day, foundational intermediates support the journey from raw bench chemicals to life-saving medicines and everyday materials.

    Supporting Facts: Why Quality Matters in Halogenated Intermediates

    Running parallel reactions with standard-purity versus high-purity 2-Bromo-6-Chloropyrazine tells a simple story: fewer purification cycles, quicker reaction monitoring, and improved yield metrics come from investing in a trusted source. The presence of trace impurities, sometimes as little as 1%, often leads to chromatographic shadows, lower crystallinity in final products, or unpredictable reactivity. For projects where analytical tracking is non-negotiable, a quality standard above 98% delivers a near-seamless bench experience. Analytics, such as NMR and HPLC, easily differentiate the genuine article from batches with poor shelf-life or break-down.

    Shipping and storage also factor in. Keeping the product well-sealed in an amber bottle, away from sunlight and high humidity, expands its usefulness over months. Long-term R&D projects benefit, since the unpredictability of a degraded lot can throw off entire timelines. One missed deadline sets back innovation, sometimes by months.

    Through in-person troubleshooting and project management, it’s clear that relying on solid intermediates—chemically and logistically—pays out both in saved time and peace of mind. Some teams try to cut corners by preparing their own halogenated precursors, but the unpredictability of side-product profiles and batch-to-batch variability brings more headache than it solves.

    Sustainability and Safety

    Environmental and personal safety can’t be left out, especially in a world shifting toward cleaner synthesis and stricter regulations. Handling 2-Bromo-6-Chloropyrazine should always follow rigorous safety procedures. Proper glove use, fume hood operation, and waste separation ensure not just compliance but also long-term well-being. The measured volatility and controlled reactivity level allow for safer reaction setup than some more volatile or unstable halogenated agents.

    Modern synthesis techniques, like flow chemistry or catalytic coupling with recyclable ligands, provide eco-friendlier routes to derivative compounds. Shifting from harsh conditions to milder protocols powered by robust substrates such as this one translates to fewer emissions and safer waste. Institutions adopting green chemistry principles can still achieve high yields and functionality thanks to smart intermediate design.

    How the Right Intermediate Transforms Research

    For the synthetic chemist, the small details in a starting material make a big difference: batch longevity, ease of monitoring, and reactivity window. Building complex, value-added structures is rarely linear or frictionless, and choosing a dual-halogen intermediate sidesteps some of the classic pitfalls—overreaction, impurity carryover, or sluggish conversion rates. A streamlined workflow frees up time for real creative work or for troubleshooting genuine surprises instead of routine failures.

    Early career researchers and veterans alike appreciate the salvageable nature of failed reactions when working with 2-Bromo-6-Chloropyrazine: if one halogen reacts ahead of schedule, the other remains available for another attempt. These backstops save both budget and morale, especially on longer-term projects or scarce funding cycles.

    Improving Sourcing and Access

    For global teams, consistent supply chains matter. Delays or shortages in key intermediates can stop a project just as productivity builds momentum. Sourcing 2-Bromo-6-Chloropyrazine from trusted suppliers helps manage inventory, balance long-term project planning, and ensures compliance with local transport and handling laws. Oversight authorities check for documentation, traceability, and handling certifications; the discipline of working with a standard intermediate makes audit processes simpler. This compliance brings peace of mind to both team leads and regulatory staff.

    Online sourcing has improved access, but direct relationships with reputable chemical distributors make a difference, especially if technical questions arise. I’ve found it useful to keep open lines of communication with sales staff and tech reps, especially when evaluating batch-specific data or troubleshooting analytical puzzles.

    Cost, Efficiency, and the Bottom Line

    Production budgets keep tightening, and time-to-market makes a real difference in competitive fields like pharma and agriculture. Choosing a modular, dual-halogen intermediate slashes the complexity of multistep projects. Internal cost-tracking from several labs shows savings not just in reagents, but in labor hours and machine use, when compared with less versatile analogs. Waste is simplified, reaction setup becomes more predictable, and final yields climb higher. Finance teams, always under the gun to do more with less, appreciate the efficiency gains that come from optimized chemistry routines.

    While upfront prices may seem higher in the catalog compared to locally-prepared or less pure variants, the break-even comes surprisingly quick after accounting for shorter run times, fewer failed batches, and reduced hazard pay for staff.

    Potential Solutions to Industry Challenges

    Supply chain challenges, safety standards, and green chemistry demands remain front and center for chemical producers and end users. A consistent and deeply characterized intermediate, like 2-Bromo-6-Chloropyrazine, supports these needs. Building relationships with reliable distributors, investing in higher purity grades, and choosing suppliers who offer transparency about production practices reduce risk and bolster long-term planning. Companies working toward sustainability can combine smart intermediate selection with modern catalytic methods—limiting reagents, lowering temperatures, and recycling solvents—to move projects forward without stalling on environmental compliance.

    Investing in lab training also keeps both people and products safer, broadening the expertise available in a team and supporting responsible stewardship of hazardous materials. For students and early-career chemists, solid training on a go-to intermediate demystifies both classic and novel reactivity, making the next generation of scientists better prepared for industry demands.

    Process automation and digitization further smooth out wrinkles in supply and use. Automated tracking of intermediate usage, real-time analytics, and integrated inventory management systems empower chemists to keep tabs on both raw materials and along-the-way results. This translates into fewer shutdowns, less wasted effort, and quicker pivots if unexpected challenges emerge.

    Looking Ahead: The Ongoing Value of Flexible Intermediates

    As research agendas grow more ambitious, the core demand for reliable intermediates rises in parallel. Synthetic chemistry is a craft in which small modifications yield huge differences in outcome. The unique profile of 2-Bromo-6-Chloropyrazine—combining reactivity, stability, and adaptability—creates a real competitive advantage. For growing enterprises and university teams alike, access to trusted starting blocks underpins sustained scientific progress.

    By focusing on the practical advantages and wide adaptability of this compound, researchers can maximize efficiency and reduce risk. Having spent days hunting for obscure reagents or troubleshooting strange byproducts, I appreciate how much a trusted intermediate simplifies daily lab work.

    In fields as demanding and fast-paced as pharmaceuticals and specialty chemicals, attention to the details of intermediate selection keeps projects on time and within budget. Choosing well-characterized, versatile reagents, like 2-Bromo-6-Chloropyrazine, makes the difference between endless workaround cycles and a streamlined path to breakthrough results.