Description

4-Chloro-2,6-difluorobenzotrifluoride (CAS No. 1221272-93-0) is a high-purity fluorinated aromatic compound with the molecular formula C₇H₂ClF₅. Its IUPAC name, 5-chloro-1,3-difluoro-2-(trifluoromethyl)benzene, reflects its precise structural configuration, featuring chloro and fluoro substituents on a benzene ring with a trifluoromethyl group. This compound is synthesized under stringent conditions to ensure exceptional quality, making it ideal for advanced research and industrial applications.

With a molecular weight of 216.54 g/mol, this chemical exhibits unique reactivity due to its electron-withdrawing substituents, making it valuable in pharmaceutical intermediates, agrochemical synthesis, and materials science. Its stability under various conditions ensures reliable performance in demanding environments. Each batch undergoes rigorous analytical testing (GC, HPLC, NMR) to confirm purity and consistency, meeting the standards of researchers and scientists.

Packaged in chemically resistant containers under inert conditions, our 4-Chloro-2,6-difluorobenzotrifluoride is supplied with comprehensive technical data, including MSDS, COA, and spectral data. Available in quantities from grams to kilograms, we cater to both small-scale research and bulk industrial needs.

Properties

• CAS Number: 1221272-93-0
• Complexity: 168
• IUPAC Name: 5-chloro-1,3-difluoro-2-(trifluoromethyl)benzene
• InChI: InChI=1S/C7H2ClF5/c8-3-1-4(9)6(5(10)2-3)7(11,12)13/h1-2H
• InChI Key: SGJLWILHBZITFS-UHFFFAOYSA-N
• Exact Mass: 215.9765186
• Molecular Formula: C7H2ClF5
• Molecular Weight: 216.53
• SMILES: C1=C(C=C(C(=C1F)C(F)(F)F)F)Cl
• Monoisotopic Mass: 215.9765186
• Synonyms: 4-Chloro-2,6-difluorobenzotrifluoride, 1221272-93-0, 5-chloro-1,3-difluoro-2-(trifluoromethyl)benzene, SGJLWILHBZITFS-UHFFFAOYSA-N, DTXSID901240032, MFCD16140186, AKOS005258181

Application

4-Chloro-2,6-difluorobenzotrifluoride serves as a versatile building block in organic synthesis, particularly in the development of fluorinated pharmaceuticals and agrochemicals. Its electron-deficient aromatic ring enables selective functionalization in cross-coupling reactions, making it valuable for drug discovery. Additionally, it is used in materials science to engineer high-performance polymers and liquid crystals with enhanced thermal and chemical resistance. Researchers also employ it as a precursor for specialty chemicals in catalysis and surface modification applications.

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