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6-Bromo-2,2,3,3-Tetrafluoro-1,4-Benzodioxan

    • Product Name 6-Bromo-2,2,3,3-Tetrafluoro-1,4-Benzodioxan
    • Alias MFCD06738073
    • Einecs 816-183-8
    • 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

    773620

    Product Name 6-Bromo-2,2,3,3-Tetrafluoro-1,4-Benzodioxan
    Cas Number 145206-94-2
    Molecular Formula C8H2BrF4O2
    Molecular Weight 287.99 g/mol
    Appearance White to off-white solid
    Purity Typically ≥97%
    Solubility Soluble in organic solvents such as DMSO, chloroform
    Smiles C1OC2=C(O1)C=C(C(=C2)Br)C(F)(F)C(F)F
    Inchi InChI=1S/C8H2BrF4O2/c9-4-2-6-14-7-3-5(8(10,11)12)1-13-7(6)4/h2-3H,1H2
    Synonyms 6-Bromo-2,2,3,3-tetrafluoro-1,4-benzodioxane
    Storage Conditions Store at room temperature, keep container tightly closed

    As an accredited 6-Bromo-2,2,3,3-Tetrafluoro-1,4-Benzodioxan factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "6-Bromo-2,2,3,3-Tetrafluoro-1,4-Benzodioxan, 5g." Features hazard symbols, CAS number, and lot code.
    Shipping 6-Bromo-2,2,3,3-Tetrafluoro-1,4-Benzodioxan is shipped in secure, leak-proof containers compliant with chemical safety regulations. Packaging is designed to prevent breakage and exposure. The product is labeled according to hazardous material guidelines and shipped with documentation specifying handling and storage requirements. Temperature and transit conditions are controlled as required.
    Storage **6-Bromo-2,2,3,3-tetrafluoro-1,4-benzodioxan** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Store separately from incompatible materials such as strong acids, bases, and oxidizers. Always keep the container clearly labeled and handle using appropriate personal protective equipment (PPE).
    Application of 6-Bromo-2,2,3,3-Tetrafluoro-1,4-Benzodioxan

    Applications of 6-Bromo-2,2,3,3-Tetrafluoro-1,4-Benzodioxan in Industrial Manufacturing

    As a direct manufacturer of 6-Bromo-2,2,3,3-Tetrafluoro-1,4-Benzodioxan, we deliver this advanced intermediate to downstream industries requiring specialized fluorinated building blocks. Below are real-world application scenarios with tailored integration details, reflecting genuine compliance requirements and typical industrial usage practices.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical firms utilize this compound as a fluorinated building block in advanced small-molecule APIs, targeting immunology and oncology treatments. The raw material enters the synthesis at the fluorination or arylation stages for actives where high metabolic stability and halogen tailoring are critical. Custom process routes shape the ratio depending on target API structure and reaction yield optimization. Quality control includes complete traceability for registered drug master files. End formulations go into clinical and commercial drug products for regulated global supply chains.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia Monographs
    • United States Pharmacopeia (USP) General Chapters
    • REACH Registration for Manufacturing/Importation

    Typical usage ratio

    • 0.5%–4.5% molar ratio, determined by specific synthetic route and molar excess for targeted coupling efficiency

    Downstream process integration

    • Introduced during the key halogenation or fluorination synthesis step as a reagent or intermediate
    • Integrated before palladium-catalyzed cross-coupling (e.g., Suzuki, Buchwald-Hartwig reactions)
    • High-purity material ensured by in-process HPLC and GC-QC release

    Final product types

    • Immunomodulator active pharmaceutical ingredients (APIs)
    • Targeted cancer therapeutic molecules
    • Experimental fluorinated oral drugs

    2. Agrochemical Active Ingredient Production

    Downstream agrochemical factories employ this raw material for the design and synthesis of next-generation herbicides and fungicides. Its electron-withdrawing properties and dual halogenation profile help tailor selectivity and persistence in crop protection formulations. Producers adjust addition ratios according to the structure-activity relationship of target compounds and seasonal crop requirements. This material is integrated into multi-step syntheses before final formulation under ISO-compliant batch control. Final products are exported under strict chemical labeling and residue control standards.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for Chemical Manufacturing)
    • FAO/WHO Guidelines on Pesticide Specifications
    • OECD/GLP for Agrochemical Testing
    • Globally Harmonized System of Classification and Labelling of Chemicals (GHS)

    Typical usage ratio

    • 3%–10% by weight per target active ingredient batch; further adjustment based on the molecule's efficacy and environmental persistence studies

    Downstream process integration

    • Added to primary synthesis as a functionalized aryl source
    • Reacted with selective coupling partners for active scaffold formation
    • Feeds into downstream formulation unit for EC, SC, or WG crop protection preparations

    Final product types

    • Herbicidal actives for resistant weed management
    • Fungicidal actives for post-harvest crop safety
    • Custom pesticide intermediates for regional agricultural sectors

    3. Specialty Fluorinated Polymer Additives

    Producers of high-performance polymers and elastomers incorporate this molecule as a chain-functionalization or co-monomer additive to modify polymer backbone characteristics. Its high fluorine content imparts hydrophobicity and thermal stability, which is critical for end-use applications in electronics and filtration. Processing engineers define addition levels during resin formation or melt-polymerization based on desired mechanical and chemical resistance properties, with batch oversight aligned to polymer-specific standards.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management System)
    • RoHS Directive (EU Restriction of Hazardous Substances)
    • ASTM D6288 (Fluoropolymer Material Standards)
    • EU REACH Regulation (Polymer Exemption, Intermediate Use)

    Typical usage ratio

    • 0.1%–3% by weight of total polymer matrix; specifications adjusted per thermal gravimetric and mechanical test data

    Downstream process integration

    • Fed into pre-polymer solution before copolymerization steps
    • Blended post-polymerization for tailored surface modification
    • Participates in extrusion or compression molding to achieve target part performance

    Final product types

    • Membrane layers for industrial filtration equipment
    • Encapsulant materials for electronic components
    • Fluorinated elastomer gaskets and seals

    4. Advanced Organic Electronics Development

    Manufacturers in the organic electronics and semiconductor sector employ this raw material within the synthesis of fluorinated aromatic compounds, targeting controlled electronic properties for OLED emitters and organic semiconductors. Its unique combination of bromine and tetrafluoro substituents provides fine-tuning potential for bandgap engineering. Developers precisely meter the input ratio for each batch based on device layer architecture. The material typically enters at early intermediate synthesis or is used in doping agents preceding final thin-film deposition.

    Industry compliance standards

    • IPC-4101 (Base Materials for High-Performance Printed Boards)
    • IEC 61249 (Materials for Printed Circuits)
    • ISO 14001:2015 (Environmental Management for Electronics Manufacturing)
    • EU REACH (SVHC Pre-screening for Electronic Device Materials)

    Typical usage ratio

    • 0.2%–1.2% by weight of the final functional layer; optimized based on desired charge transport and emissive properties

    Downstream process integration

    • Introduced in the synthesis of precursor molecules before conversion to charge transport materials
    • Used as a source of fluorinated aromatic units in solution-based deposition workflows
    • Integrated into doping solution for vapor phase or spin-coating steps

    Final product types

    • OLED microdisplay emitter compounds
    • Organic field-effect transistor semiconductors
    • Flexible printed circuit materials for smart devices
    Free Quote

    Competitive 6-Bromo-2,2,3,3-Tetrafluoro-1,4-Benzodioxan prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 6-Bromo-2,2,3,3-Tetrafluoro-1,4-Benzodioxan – Manufacturer’s Perspective

    What 6-Bromo-2,2,3,3-Tetrafluoro-1,4-Benzodioxan Brings to a Chemist’s Bench

    The market for halogenated aromatics continues to evolve as new demands appear in advanced materials, pharmaceuticals, and functional polymers. Out on the production floor, we know why certain compounds stand out once you get hands-on with them. 6-Bromo-2,2,3,3-tetrafluoro-1,4-benzodioxan serves as a prime example. With the CAS number 866348-75-6, this molecule offers a blend of reactivity, metabolic stability, and electronic properties that are hard to find in one package.

    Our plant has years of experience scaling up fluorinated aromatic compounds. The advantages of introducing two pairs of gem-difluoro groups to the benzodioxan system, then anchoring a bromine atom on the ring, become pretty clear. In every shift, we see the consistency required for downstream reactions. The tetrafluoro substitution gives the backbone resistance to metabolic breakdown; the bromo moiety unlocks versatile cross-coupling opportunities in Suzuki, Stille, or Ullmann-type protocols. A single batch can support both medchem lead-optimizations and advanced organic synthesis for electronic materials.

    Why Structure Matters Beyond the Lab Notebook

    A lot of engineers ask us what sets our 6-bromo-2,2,3,3-tetrafluoro-1,4-benzodioxan apart from related products in this segment. Benzodioxans without fluorine do appear in some catalogues, but they respond very differently under reaction conditions. Fluorine introduces strong electron-withdrawing effects, which extends to raising thermal and oxidative stability. In our reactor systems, this translates to a compound that withstands higher temperature polymerizations and aggressive halogenation without falling apart or decomposing.

    Brominated benzodioxans without fluorine find use as intermediates, but their byproducts can be tricky. Our material, purified and analyzed by our in-house team, has clear advantages due to minimal side-reactions and high selectivity during further synthetic steps. This brings savings to process developers and medicinal chemistry programs. The tetrafluoro groups also drop the basicity of the ring, narrowing possible isomeric byproducts. On our site, spectral QA includes 1H, 13C, and 19F NMR data bundled with shipment, a step developed through real-world batch feedback.

    Typical Specifications and Plant Realities

    6-Bromo-2,2,3,3-tetrafluoro-1,4-benzodioxan runs as a crystalline solid, pure white, with melting points matching published data. Recrystallization and trace element scans help us control heavy metal content and organic impurities. For each production run, we record GC and HPLC purity levels above 98%. We’ve learned that some competitors skip the double-fine filtration step, often resulting in off-white byproduct. We sided with finer filtration even though it slows batch turnaround, because feedback from polymer and pharma clients consistently favored this over small savings in production time.

    Moisture content stays consistently below 0.2% by Karl Fischer titration. We pack each shipment under nitrogen, heat-sealed and labeled automatically. Long-term stability — a regular concern for research and bulk buyers alike — benefits from the fluorinated scaffold. Even after months in warehouse storage, customers report unchanged reactivity and no browning or breakdown when the containers stay intact.

    Where Chemists Use This Molecule

    Medicinal and process chemists reach out for our fluorinated benzodioxan mostly for its selective reactivity. In pharmaceutical intermediates, the introduction of both electron-rich and electron-deficient zones allows for a broad swath of Suzuki and Sonogashira reactions. One of our daily customers scales up aryl amines with a late-stage bromo replacement, thanks to the anchoring effect of two pairs of CF2 groups. The result – faster lead optimization and fewer partial dehalogenation problems.

    Developers of specialty polymers and advanced coatings use it in monomer feeds to create high-performance resins. The 1,4-benzodioxan core provides aromatic stability, while the tetrafluoro substitutions minimize unwanted cross-linking during polymer growth. Thin film electronics developers see direct benefits, since the electron-poor ring reduces charge trapping in dielectric layers. We see growing interest from OLED and organic solar cell manufacturers for these same reasons.

    Exploring Synthetic Pathways and Scalability

    Scaling up halogenated fluorobenzenes presents challenges that go beyond tricks in academic literature. We adapted and tuned our process routes to minimize waste streams, avoid unstable intermediates, and run at moderate pressures. Starting from catechol, our established pathway introduces the bromo and tetrafluoro substituents in a controlled sequence, with selectivity controlled by temperature and choice of fluorinating agents. Unlike some global competitors, we keep the same solvent mix through both halogenation steps, cutting down on cross-contamination and solvent disposal costs.

    Yield, efficiency, and purity dominate our process design. Our floor operators rejected attempts at using milder fluorinating conditions after seeing a steady increase in mixed halogen byproducts. The more direct fluorine source we adopted — trialed, analyzed, and tuned by our analytical chemists on site — paid off with shorter cycle times and higher batch consistency. Over the years, adopting in-line IR and deep-dive NMR monitoring further cut batch waste and let us spot impurity trends before product hits the final drum.

    How Differences Impact User Choice

    Many procurement teams look at surface features or purity numbers when scouting for fine chemicals, but our colleagues in the lab are quick to spot subtle differences. Brominated benzodioxans without fluorine are cheaper but rarely survive the same range of reaction conditions. By introducing both tetrafluoro and bromo groups, we offer a molecule that lets chemists push more temperature, more reaction cycles, and still collect clean product.

    Compounds with only mono-fluorination lack the same stability in oxidative environments, often showing side-reactions in scale-up runs. Our tetrafluoro version prevents these headaches, as seen in several process validation projects with pharmaceutical partners. Paper data and commercial claims only tell part of the story. The actual ease of alkylation and cross-coupling shows up once production switches over to this batch – fewer adjustments, increased throughput, and less need for in-process purification.

    For electronics and materials research, the cumulative effect of just a few extra halogen atoms can define dielectric performance and resistance to long-term stressors. Teams running thin film deposition or polymer casting found measurable improvements in device reliability over six months of aging tests. Organic solar cell developers sent us back side-by-side comparisons of products with and without the extra fluorine — and the durability and charge transport improvement stood out in every trial.

    Customer Experience and Long-Term Supply Relationships

    Most new buyers ask about historical supply consistency. Over the last several years, our records show stable output and batch-to-batch purity tracking. Academic groups have published results citing material sourced directly from our reactors. These collaborations pushed us to adapt production to more demanding trace impurity limits, especially for projects targeting regulatory approval. One medchem client started in lead optimization and, after multiple successful SAR cycles, now runs pilot-scale synthesis based on our standard material. They’ve told us how late-stage bromo substitution on such a stable scaffold sped up analog development and reduced analytical headaches.

    We pay attention to frequent shipment requests for smaller, fresh-packed lots. Many high-value projects want smaller quantities, but with full documentation and support. On any given month, almost one third of our lots ship in custom-sized containers, accompanied with complete analytical data and Certificate of Analysis covering every QA metric tracked on-site. Our packing team reviews each customer’s feedback to tune container size, desiccant, and labeling. Feedback coming from actual product users matters more to production than sales statistics or generic survey info.

    Operational Safety, Logistics, and Compliance on the Manufacturer’s End

    The safety profile of halogenated, fluorinated benzodioxans does not match the simpler aromatics. Training and real practice in our plant undergirds each material transfer. We’ve invested in local extraction hoods and sealed reactor systems because even minor inhalation can become a regulatory event and a health risk. From the operator’s perspective, accuracy in weighing, drying, and dispatch means fewer rework cycles, less team exposure, and a lot fewer late-night calls from logistics.

    Storage and transit receive the same attention from our logistics crew as synthesis. We run shelf-life studies internally. Everything ships in moisture-tight, labeled packages under nitrogen. Governing transport and customs regulations treat this compound as a specialty chemical — and we interact with all documentation first-hand, not through agents or brokers. Buyers appreciate not having to chase down safety data or import codes mid-shipment. In jurisdictions with additional environmental or pharma regulations, we work closely with client compliance teams to build a paper trail that passes legal and regulatory review.

    Continuous Improvement and Customer-Led Innovation

    Plants do not stand still, especially in our segment. Customers bring us new demands every year. We’ve shifted purification protocols based on the way our products perform in new synthetic or engineering applications. A customer testing fluorinated benzodioxans for PET track-etch membranes reported that tighter particle size control led to better surface results. We changed crystallization and drying steps to deliver more consistent lots, tracking particle distribution more closely and fine-tuning our sieves and dryers. Another client in lithium battery research reported that their non-standard electrolyte reviews required a more detailed breakdown of trace residues, and we adapted batch documentation and analytical reporting to reflect this.

    Our technical support team fields detailed application support requests backed by real batch records, plant trial data, and analytic runs done on-site. Scientific literature on complex halogenated aromatics often lags, but customers in advanced materials, OLED research, and life science intermediates rely on our production data and experience scaling up uncommon structures. We take pride in responding directly, not with scripted responses but with information drawn from our own processes, pilot-scale trials, and hands-on expertise.

    Supply Security in an Uncertain Market

    Shortages in raw fluorination agents or brominating reagents affect supply across our industry. With years of vendor relationships and on-site purification capability, we keep backup stocks and quality-tracked supplier networks. During recent years, we made investments in cold storage, stability monitoring, and contingency shipments to avoid interruptions and keep price volatility to a minimum. Large bulk buyers appreciate knowing that reserves are not dependent on short-term imports or low-cost intermediates. We run an audit trail on every incoming raw material and work closely with analytical groups to ensure that finished lots meet the same strict standards, shipment after shipment.

    Looking Forward — What Experience Teaches

    Bringing 6-bromo-2,2,3,3-tetrafluoro-1,4-benzodioxan from a digital structure to a drum on your loading dock involves more than purity stats and spec sheets. Developing this product line called for investments in equipment, operator training, analytical instrumentation, and a willingness to respond directly to real client needs. The most important lesson is that living data from real-life performance ultimately shapes manufacturing choices. We have advanced formulation teams, process chemists, and QA staff working together under one roof — they know that every customer batch, every test report, adds up over time.

    In laboratory notebooks and production reports alike, performance data always wins out over theory. That is why our 6-bromo-2,2,3,3-tetrafluoro-1,4-benzodioxan became a preferred choice for demanding pharmaceutical, electronics, and materials research clients. Our focus on structure, process transparency, and flexibility in custom lots ensures that chemists and engineers relying on our product gain real-world advantages. Supply reliability, thorough analytics, and readiness to innovate or adapt to end-user needs form the bedrock of our approach today and set our direction for the future.