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HS Code |
190603 |
| Chemicalname | 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene |
| Molecularformula | C8H4F4N2O2 |
| Molecularweight | 236.12 g/mol |
| Casnumber | 342879-86-3 |
| Appearance | White to off-white solid |
| Solubility | Soluble in common organic solvents |
| Purity | Typically ≥ 97% |
| Smiles | Nc1cc2oc(cc2oc1F)F |
| Inchi | InChI=1S/C8H4F4N2O2/c9-8(10)5-3-13-6-2-1-4(12)7(14-6)11-5/h1-3H,12H2 |
| Storagetemperature | Store at 2-8°C |
As an accredited 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 mg of 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene, sealed in an amber glass vial with tamper-evident cap, labeled. |
| Shipping | 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene should be shipped in tightly sealed containers under dry, cool conditions. Handle and transport as a hazardous chemical, following all relevant regulations for toxic and potentially environmentally harmful substances. Avoid physical damage, excessive heat, and direct sunlight. Proper labeling and documentation must accompany the shipment. |
| Storage | 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Use chemical-resistant containers, and label clearly. Access should be restricted to trained personnel, with proper personal protective equipment available nearby. |
Applications of 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene in Industrial ManufacturingWe supply 2,2,3,3-Tetrafluoro-5-Amino-1,4-Benzodioxene, which has enabled new advances in specialty organofluorine chemistry. Below, we detail downstream applications where this intermediate forms an essential and differentiated role. Each scenario below draws from commercially validated production models, with focused discussion of industry compliance, formulation, process flow, and product output. 1. Advanced Pharmaceutical Intermediate SynthesisMajor pharmaceutical companies use this fluorinated benzodioxene as a key amine-containing building block when synthesizing heterocyclic scaffolds for selective kinase inhibitors and antiviral drugs. Its electron-withdrawing and sterically hindered properties help improve drug candidate stability during complex multi-step syntheses. Downstream integration mainly appears in the late intermediate coupling stages during small molecule API (active pharmaceutical ingredient) manufacturing for advanced therapeutic candidates. Industry compliance standards
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2. Fluorinated Specialty Polymer SynthesisLeading electronics and membrane manufacturers use this compound as a highly effective polycondensation monomer for synthesizing high-performance polymers with strong thermal and solvent resistance. It delivers improved dielectric properties and chemical inertness, which are critical for advanced filtration membranes and thin-film applications. The raw material gets incorporated during the polycondensation reaction, predominantly forming part of the backbone in aromatic copolymers. Industry compliance standards
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3. Agrochemical Active Ingredient IntermediateAgrochemical R&D and production teams introduce this aminated, heavily fluorinated intermediate when constructing new classes of crop protection actives, specifically for developing fungicides with strong field persistence and reduced mammalian toxicity. The material is integrated in the early to mid-stage pathway for assembling fused heterocyclic structures common to next-generation systemic fungicides. Quality documentation and exposure controls require full traceability throughout the downstream synthesis workflow. Industry compliance standards
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4. OLED Material IntermediateDisplay panel manufacturers and materials formulators apply this specialty compound as a precursor for creating blue- and green-emitter fluorinated organic semiconductor materials. The amine functionality, combined with the tetrafluoro substitution, tailors emission wavelength and enhances oxidative stability needed in high luminance OLED construction. Use is focused on fine chemical synthesis for constructing emitter cores or electron transport layers, with purity and heavy metal trace limits stringently monitored for panel reliability. Industry compliance standards
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5. Performance Coating Resin ModificationCoatings manufacturers incorporate this benzodioxene derivative as a resin modifier to introduce fluorine content, substantially increasing chemical and UV resistance in functional coatings. Its reactive amino group facilitates copolymerization or crosslinking with epoxy or acrylic resins, while the tetrafluoro groups help minimize surface energy and migration of aggressive chemicals. The compound typically enters at the oligomer building or curing stage to impart end-use durability for specialty industrial surfaces. Industry compliance standards
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