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5-Bromo-2-Chloroanisole

    • Product Name 5-Bromo-2-Chloroanisole
    • Alias 2-Chloro-5-bromoanisole
    • Einecs 620-556-7
    • 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

    250815

    Chemical Name 5-Bromo-2-Chloroanisole
    Molecular Formula C7H6BrClO
    Molecular Weight 237.48 g/mol
    Cas Number 54304-97-1
    Appearance Colorless to pale yellow liquid
    Boiling Point 256-258°C
    Melting Point Unknown
    Density 1.62 g/cm³
    Purity Typically ≥98%
    Solubility Insoluble in water
    Smiles COC1=C(C=C(C=C1)Br)Cl
    Refractive Index 1.573

    As an accredited 5-Bromo-2-Chloroanisole 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-2-Chloroanisole

    Applications of 5-Bromo-2-Chloroanisole in Industrial Manufacturing

    5-Bromo-2-Chloroanisole supports advanced synthesis and value chain extensions across agrochemicals, pharmaceuticals, specialty intermediates, electronic chemicals, and dye intermediates. Our facility provides tailored purity control, particle size, and packaging options for demanding downstream workflows. Below we detail key application sectors supported by this chemical intermediate.

    1. Agrochemical Synthesis: Key Building Block for Selective Herbicides

    Leading agrochemical producers use 5-Bromo-2-Chloroanisole as a halogen source in synthesizing active herbicidal compounds, especially for selective weed management in cereal crops. It introduces bromo and chloro functionalities into aromatic rings, enabling the construction of target-specific active ingredients. Production lines incorporate it in high-efficiency coupling and substitution steps, accelerating synthesis while minimizing by-products. Advanced purification and controlled reaction conditions maintain required residual thresholds for export-grade formulation batches.

    Industry compliance standards

    • FAO/WHO specifications for pesticide active ingredients
    • ISO 17025 laboratory testing accredited procedures
    • China GB/T 1601-2015 agrochemical raw material standards
    • REACH regulation (EC) No 1907/2006 for European registration

    Typical usage ratio

    • 2.5%–12% relative to total reactant charge per batch, adjusted for target herbicide pathway and desired halogenation extent

    Downstream process integration

    • Batch introduction at nucleophilic aromatic substitution or Suzuki coupling step as the bromo-chloro arene substrate
    • Participates in multi-step synthesis with real-time inline chromatographic purity checks for critical intermediate control

    Final product types

    • Selective herbicides for wheat, rice, and corn applications
    • Pre-emergent and post-emergent weed control agents
    • Custom pesticide formulation intermediates

    2. Pharmaceutical Intermediate: Precursor for API Halogenation

    Active pharmaceutical ingredient manufacturers rely on 5-Bromo-2-Chloroanisole in the preparation of halogenated aromatic scaffolds, supporting the synthesis of antihypertensive, anti-inflammatory, and neuroactive APIs. It enters multi-step synthesis campaigns where halogen patterning is required to obtain pharmacologically suitable aromatic motifs. Process engineers utilize analytical-grade material to maintain impurity control, essential for later GMP-compliant finishing. Rigorous traceability from incoming raw material enables full documentation during DMF submission and regulatory audits.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF and EP guidelines for chemical raw materials
    • China Drug Master File (DMF) registration rules
    • FDA cGMP 21 CFR Part 211

    Typical usage ratio

    • 0.5–5 molar equivalents per API batch, determined by specific route and scale of halogen insertion

    Downstream process integration

    • Incorporated at initial or mid-stage halogenation step to build complex aromatic intermediates
    • Subjected to additional protection, deprotection, or further functional group introduction as process advances

    Final product types

    • Halogenated pharmaceutical actives (e.g., antiarrhythmic drugs, CNS agents)
    • Research compounds and clinical trial intermediates
    • Generic API intermediates exported to regulated and semi-regulated markets

    3. Electronic Chemicals: Intermediate for Liquid Crystal Monomers

    Prominent electronic materials makers use this compound during the production of advanced liquid crystal monomers for LCD and OLED panel manufacturing. Its unique halogen profile prompts distinctive mesogenic properties after incorporation via precise Suzuki and Stille coupling reactions. Stringent process filtration and material handling maintain trace metallic and halide contaminants at sub-ppm levels to comply with display industry reliability requirements. Material is offered in custom particle sizes for high-throughput microreactor and continuous manufacturing systems.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic chemical substances
    • IEC 61249 base material and impurity limitations
    • Japanese Electronic Industry Standard (JIS C5016)
    • REACH registered for use in electronics supply chain

    Typical usage ratio

    • 1.5%–6.5% by weight in coupling feedstock, scaled according to desired monomer substitution density

    Downstream process integration

    • Charged as halogen source during mesogen core functionalization, followed by purification
    • Used in small-molecule and polymeric LCD monomer synthesis, then passed to blending and alignment process

    Final product types

    • High-performance liquid crystal materials for display panels
    • LCD and OLED alignment layers
    • Specialty electronic inks and patterning agents

    4. Dye and Pigment Intermediate: Source Material for Azo and Anthraquinone Dye Production

    Specialty colorant manufacturers incorporate 5-Bromo-2-Chloroanisole as a halogenated aromatic nucleus during azo and anthraquinone dye synthesis. It enables targeted bromine and chlorine placement to adjust chroma, fastness, and solubility properties of industrial dyes. Manufacturing lines deploy controlled coupling and diazotization sequences at elevated temperatures, enabling precise control over by-product profiles. Process controls track material lot numbers, and dedicated equipment is used to prevent passive cross-contamination with non-halogenated dye streams.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Restricted Substances List
    • ISO 9001:2015 Quality Management for pigment intermediates
    • EU Regulation (EC) No 1907/2006 REACH for colorants
    • China GB/T 21899-2008 for dye intermediates

    Typical usage ratio

    • 5%–17% by weight of reaction charge, adjusted based on pigment class and target color intensity

    Downstream process integration

    • Charged to azo coupling or anthraquinone ring-closure steps to introduce halogen diversity
    • Incorporated early in synthesis to ensure halogen groups are preserved through finishing

    Final product types

    • Reactive and disperse textile dyes with enhanced fastness
    • High-performance pigments for inks and coatings
    • Colorants used in plastics and technical fibers

    5. Fine Chemical Intermediates: Building Block for Custom Organic Synthesis

    Custom synthesis and contract manufacturing operations value 5-Bromo-2-Chloroanisole for generating novel heterocyclic and aromatic structures. Chemists use it as a key substrate for molecular diversification by cross-coupling, halogen-metal exchange, and directed ortho-metallation. Its unique substitution pattern opens synthetic access to materials for research, catalysis, and high-value specialty intermediates. We provide full batch traceability, supply collaborative development services, and offer tailored packaging for kilo-lab to pilot scale up.

    Industry compliance standards

    • ISO 9001:2015 for development and manufacturing of fine chemical intermediates
    • GHS labeling and transport compliance
    • IUPAC nomenclature and analytical characterization protocols
    • Custom documentation packages for technology transfer and regulatory submissions

    Typical usage ratio

    • 10%–20% by mol in specialized reaction screens, scaling based on target molecule and side-chain installation

    Downstream process integration

    • Entered at early scaffold-building stage for halogenated derivative libraries
    • Subjected to metal-catalyzed coupling, nucleophilic displacement, or downstream functionalization depending on target

    Final product types

    • Heterocyclic precursors for flavor and fragrance engineering
    • Electronic material intermediates and organic semiconductor bases
    • Custom research molecules for academic and industrial labs
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    More Introduction

    Introducing 5-Bromo-2-Chloroanisole: A Niche Chemical with Big Impact

    A Close-Up Look at 5-Bromo-2-Chloroanisole

    After spending years in labs and chemical synthesis environments, certain molecules stick out for their versatility. 5-Bromo-2-Chloroanisole grabs attention for that very reason. Its structure, carrying both a bromine and a chlorine atom on the anisole skeleton, sets it apart from typical halogenated aromatics. For a molecule weighing in at about 235.49 g/mol, it packs a punch in selectivity and application. Its CAS number, 306934-79-4, is often recalled by researchers eager to work with something that promises consistency and reliability for particular types of work.

    Where 5-Bromo-2-Chloroanisole Comes Into Play

    Chemistry, especially on the organic side, isn’t just about mixing chemicals and seeing what happens. The devil lies in the details—adding just the right substituent at the right place can turn a bland building block into a molecular superstar. 5-Bromo-2-Chloroanisole excels in this respect. Medicinal and agrochemical teams often reach for it in the hope of starting a synthesis route that needs precise regioselectivity. The presence of both halogens next to the methoxy group shapes its reactivity in cross-coupling reactions, turning it into a favorite for introducing complexity without running into unstable side-products.

    A Question of Purity and Form

    In the world of specialty chemicals, purity often trumps all else. Researchers and process chemists can recall projects that veered off course just because a reagent turned out to be less pure than advertised. 5-Bromo-2-Chloroanisole arrives as a white to off-white crystalline powder, and its melting point—usually reported between 56°C and 59°C—is a key marker for identity and quality. High-purity grades often boast GC and NMR data that leave little doubt about what’s in the flask. This level of scrutiny reflects the high stakes: a small drop in purity, and a cascade of unreliable results can follow, costing precious time in high-value research endeavors.

    Unique Features and What Sets it Apart

    Choosing between halogenated anisoles often sparks debate inside laboratories. Some go for 4-bromo-2-chloroanisole or 2,5-dibromoanisole, but the arrangement of the bromine and chlorine in 5-Bromo-2-Chloroanisole changes the game. Chemists find that the ortho-methoxy and meta-chlorine positioning tunes electronic properties and steric hindrance just enough to steer reactions toward specific products. This sort of precision can make or break a key step in synthesizing a new compound, especially when one seeks to optimize both yield and purity. Unlike simpler anisoles, it reduces the risk of side reactions like over-halogenation, offering a more controlled pathway to downstream intermediates.

    Applications Beyond the Obvious

    The story doesn’t end at synthesis intermediates. Through collaborations and published literature, 5-Bromo-2-Chloroanisole finds its way into advanced material development and sometimes niche fragrance and flavor chemistry. Its aromatic profile—subtle but present—along with the dual-halogen functionality makes it flexible as a building block for complex organic frameworks. Certain dye and pigment manufacturers selectively use it to tweak lightfastness or solvent resistance. And in graduate-level labs, it sometimes serves as a probe to model reaction kinetics for palladium-catalyzed couplings. Each use-case expands the molecule’s reputation as one of those unsung organic chemistry tools that quietly power scientific progress.

    Handling and Storage: Lessons from Experience

    Long-term users of 5-Bromo-2-Chloroanisole know that good outcomes start with best practices in handling. It handles much like other chlorinated aromatics—dry, well-sealed containers, and away from direct sunlight. Stability isn’t an issue for typical lab usage, but careless handling can allow moisture to creep in, which in rare cases may affect both weight and purity. Some researchers, burned by a spoiled batch, have learned to segregate it from basic or strongly acidic reagents to keep it in pristine condition. Simple measures like using desiccants and tightly closing the cap after sampling prove more effective than elaborate protocols.

    Navigating Regulatory and Safety Terrain

    Regulation around specialty chemicals evolves frequently, as any frequent purchaser knows. 5-Bromo-2-Chloroanisole’s profile presents relatively modest risks compared to polychlorinated biphenyls or reactive acyl halides, but gloves and goggles remain non-negotiable in daily use. Data from hazard documentation identifies it as irritant, not as a chronic toxin. Practical lab routines—good ventilation, glove changes, and working behind a screen during transfers—offer adequate protection. Disposal follows accepted norms for halogenated organic waste: segregate, label, and let licensed handlers manage the rest. Cautious practices not only protect individual researchers but also help labs meet evolving compliance standards. Labs that cut corners find themselves dealing with administrative headaches rather than breakthrough discoveries.

    Sourcing: Reliability Above All

    Sourcing reliable 5-Bromo-2-Chloroanisole separates top-tier labs from mid-pack operations. A quick online check reveals dozens of suppliers, but not all maintain the necessary standard of documentation and consistency. Seasoned chemists share stories of ordering from less-vetted vendors only to receive material off by more than 5% in purity, or worse, contaminated by related aromatic compounds that clog synthetic workflows. Selecting suppliers who provide full traceability, batch analysis reports, and even retention samples pays off in smoother projects. In some regions, custom synthesis routes supplement bulk supply, especially when larger projects risk depleting standard stocks or when ultra-high purity becomes a non-negotiable demand.

    Comparing Alternatives: The Reason for Choosing This Molecule

    Why reach for 5-Bromo-2-Chloroanisole over something simpler or more widely available like 4-bromoanisole? The difference boils down to performance in multi-step synthesis. In cross-coupling scenarios, researchers see improved selectivity and desired functional group compatibility—a direct result of its unique halogen pattern. Some analogs offer a lower barrier of entry, but their reactivity profile doesn’t deliver the same degree of tunability, especially in reactions requiring fine control over aromatic substitution positions. This unique balance between reactivity and selectivity puts it on the short list for critical, high-yielding steps where failure means project setbacks and wasted material.

    Cost Considerations

    Ever chased the cheapest reagent, only to have it halt a project? Chemists working with 5-Bromo-2-Chloroanisole understand the calculation: quality overshadows price. Lower-quality alternatives may seem attractive on paper. In practice, they can cost far more in lost yield or repeated purification steps. The upfront investment in a lot with full analytical documentation pays dividends when projects reach production scale, or when regulatory review demands a full chain-of-custody report. CFOs and lab heads alike find themselves buying higher grades not out of luxury, but necessity.

    Scaling for Industry: From Bench to Bulk

    Transitioning a promising molecule from the research bench to industrial scale calls for more than a simple increase in batch size. 5-Bromo-2-Chloroanisole proves its worth in this arena as well. Its solid, easily handled form reduces loss during weighing and transfer. Its well-characterized melting point simplifies process monitoring. Manufacturers looking to produce kilogram or ton-scale batches find confidence knowing its reactivity profile has been well-mapped in academic and patent literature. Glass-lined reactors and controlled addition rates keep yields high and unwanted byproducts low, streamlining scale-up without the drama that plagues less predictable intermediates.

    A Sustainable Outlook

    If chemical science is to meet the needs of tomorrow, it faces the twin challenges of efficiency and sustainability. Historically, halogenated aromatics have drawn scrutiny for environmental persistence. The specific reactivity of 5-Bromo-2-Chloroanisole means that when used judiciously and recovered through distillation or crystallization, waste can be minimized. Modern labs increasingly build recovery and recycling practices into their workflow, reducing environmental load while squeezing more value from each gram purchased. The thoughtful use of such molecules points not only to good science, but also to a growing awareness that the era of disposable chemistry is ending.

    Discovery and Future Opportunities

    The chemical world moves quickly. More often than not, discovery in one area spills benefits into another. 5-Bromo-2-Chloroanisole sits at an intriguing intersection; it offers enough complexity for innovative medicinal chemistry projects, yet remains manageable for routine syntheses. Young researchers, guided by mentors who stress creative thinking, find it a perfect starting point for pushing novel reaction pathways or optimizing established ones. Cross-pollination happens: what began as an attempt to make a simple ether might open the door to more efficient catalysts or new classes of biologically active compounds.

    Collaborative Value

    Breaking silos makes chemistry stronger. In practice, some of the best work with 5-Bromo-2-Chloroanisole grows out of multidisciplinary collaborations. Synthetic organic chemists, process engineers, and analytical teams each bring a unique perspective. Where one group sees a synthetic challenge, another sees an opportunity for cleaner separations or easier waste handling. Having such an adaptable compound on hand encourages different specialties to talk, experiment, and build knowledge together. It’s this spirit of shared challenge and mutual respect that pushes research groups to take small building blocks and turn them into meaningful innovations.

    Education and Training: Teaching with Real Examples

    Good teaching draws on real-world cases, not just textbook theory. Introducing 5-Bromo-2-Chloroanisole to students exposes them to all the wrinkles of high-level lab work: understanding handling risks, verifying purity, chasing synthetic efficiency, and troubleshooting failures. Novices learning the ropes see how chemical intuition grows with hands-on experience. Graduate seminars, hackathons, and group meetings that feature this molecule wind up fostering curiosity about regioselectivity, electronic effects, and process reliability. The point isn’t just to make reactions run; it’s to train up-and-coming scientists who know why those reactions matter.

    Facing Challenges: Real-World Problems and Practical Solutions

    No chemical intermediate solves every problem without a fight. Even such a flexible molecule runs into challenges. At times, scale-up operations hit roadblocks: supply chain hiccups, variable purity across lots, or environmental concerns tied to halogenated waste streams. Progress comes from open communication between purchasers, synthetic teams, and environmental officers. Some facilities have invested in in-house analytics to catch subpar lots early. Others foster supplier relationships grounded in clear expectations—analytical support and rapid issue resolution matter as much as price point. Ongoing training and investment in greener disposal methods not only smooth rough patches but also future-proof operations as regulations evolve.

    Moving Forward: What the Future May Hold

    The world of advanced organic synthesis keeps changing. With every new class of catalysts, solvent protocols, and regulatory standards comes opportunity to build better, more cost-effective processes. Molecules like 5-Bromo-2-Chloroanisole bridge current practice with forward-thinking innovation. In the last decade, palladium-catalyzed couplings have transformed how certain drugs and agrochemicals come together. The ever-increasing demand for high-purity, selectively functionalized starting materials suggests this compound—and ones like it—will only grow in relevance. As sustainable practices become the norm, manufacturers will refine both supply-chain oversight and waste minimization, letting bench scientists focus on discovery rather than troubleshooting.

    Conclusion: The Quiet Workhorse for Today’s—and Tomorrow’s—Chemical Challenges

    There’s a tendency in chemical catalogues to skip over the essentials in favor of showy breakthroughs. Yet, the humble, high-purity crystalline solid on a shelf may be powering more innovation than anyone realizes. In hundreds of labs, 5-Bromo-2-Chloroanisole builds the molecules behind next-generation medicines, smarter materials, and safer agricultural products. Its strengths come from a unique mix of reliability, selectivity, and broad compatibility—tested daily at the hands of real working scientists. The best practitioners never take such tools for granted; they respect how much hinges on a well-chosen component and remain alert to improving safety, sustainability, and performance at every turn.