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HS Code |
662579 |
| Productname | 2,2-Difluoro-2-Phenylacetamide |
| Casnumber | 851385-70-5 |
| Molecularformula | C8H7F2NO |
| Molecularweight | 171.14 |
| Appearance | White to off-white solid |
| Purity | Typically >98% |
| Smiles | C1=CC=CC=C1C(C(F)F)N |
| Inchi | InChI=1S/C8H7F2NO/c9-8(10,7(11)12)6-4-2-1-3-5-6/h1-5H,(H2,11,12) |
| Storagetemperature | Store at room temperature |
| Synonyms | 2,2-Difluoro-2-phenylacetamide |
As an accredited 2,2-Difluoro-2-Phenylacetamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a 25g amber glass bottle with a secure cap, labeled "2,2-Difluoro-2-Phenylacetamide, ≥98%," including hazard symbols. |
| Shipping | 2,2-Difluoro-2-Phenylacetamide should be shipped in tightly sealed containers, protected from light and moisture, and stored at room temperature. Handle with appropriate safety precautions, including labeling for laboratory use. Follow all relevant regulations for chemical shipping, including UN, IATA, and OSHA guidelines. Avoid extreme temperatures and ensure secondary containment during transport. |
| Storage | 2,2-Difluoro-2-Phenylacetamide should be stored in a cool, dry, and well-ventilated area away from sources of heat, ignition, and incompatible materials such as strong oxidizers. Keep the container tightly closed and properly labeled. Store at room temperature and protect from moisture and direct sunlight. Use chemical-resistant gloves and safety equipment when handling to avoid inhalation, ingestion, or skin contact. |
Applications of 2,2-Difluoro-2-Phenylacetamide in Industrial ManufacturingAs a dedicated manufacturer, we produce 2,2-Difluoro-2-Phenylacetamide for specialized industrial applications where strict quality oversight and compliance are essential. Our material supports advanced synthesis processes for high-value downstream products in tightly regulated sectors. Explore in detail how specific industries benefit from the unique chemical properties and performance profiles of this amide derivative. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers use 2,2-Difluoro-2-Phenylacetamide as a key intermediate during the preparation of certain fluorinated drug candidates, particularly in the synthesis of new-generation CNS-active and anti-cancer molecules. The presence of both difluoro and phenyl motifs allows for late-stage diversification, supporting scaffold elaboration while maintaining compliance with stringent API impurity controls. During multi-step synthesis, this intermediate provides controlled reactivity in arylation and amidation steps before purification, as monitored by validated HPLC procedures. Industry compliance standards
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2. Agrochemical Lead Derivative Production2,2-Difluoro-2-Phenylacetamide supports the development of advanced agrochemical active ingredients by enabling the synthesis of difluorinated seed compounds with optimized physicochemical properties such as increased bioavailability and metabolic resistance. In this sector, R&D divisions incorporate the material during the early phases of active lead discovery and pilot-scale up, ensuring product performance meets or exceeds regulatory residue specifications for field applications. Industry compliance standards
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3. Specialty Fluorinated Material SynthesisIn specialty chemicals manufacturing, particularly for high-performance polymers and additives, formulators leverage the distinctive reactivity profile of 2,2-Difluoro-2-Phenylacetamide to introduce fluorinated aromatic moieties at critical linkage points within polymers or additive structures. This improves bulk material properties such as chemical durability and thermal resistance. During resin or additive scaling, the compound proves valuable in achieving precise monomer ratios and end-group modifications. Industry compliance standards
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4. Advanced Organic Synthesis ReagentsOur customers in contract research and development select 2,2-Difluoro-2-Phenylacetamide for its utility as a reagent in advanced organic transformations, including selective C–N bond formation and asymmetric synthesis required for chiral fine chemicals. Its electron-withdrawing difluoro group can modulate reactivity and selectivity when building complex aromatic frameworks, supporting efficient route selection and streamlined purifications by scalable crystallization or extraction techniques. Industry compliance standards
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