Atomfair 2,2-Difluoro-2-(fluorosulfonyl)acetic acid C2HF3O4S

Description 2,2-Difluoro-2-(fluorosulfonyl)acetic acid (CAS No. 1717-59-5) is a highly specialized fluorinated sulfonyl compound with the molecular formula C2HF3O4S. This chemical is characterized by its unique difluoroacetic acid backbone coupled with a reactive fluorosulfonyl group, making it a valuable intermediate in advanced synthetic chemistry and materials science. With a purity grade suitable for research and industrial applications, this compound is rigorously tested to ensure consistency and performance. Ideal for use in electrophilic fluorination, polymer modification, and as a precursor for sulfonyl-based reagents, it is supplied in high-quality packaging to maintain stability and integrity. Store in a cool, dry place under inert…

Description

2,2-Difluoro-2-(fluorosulfonyl)acetic acid (CAS No. 1717-59-5) is a highly specialized fluorinated sulfonyl compound with the molecular formula C₂HF₃O₄S. This chemical is characterized by its unique difluoroacetic acid backbone coupled with a reactive fluorosulfonyl group, making it a valuable intermediate in advanced synthetic chemistry and materials science. With a purity grade suitable for research and industrial applications, this compound is rigorously tested to ensure consistency and performance. Ideal for use in electrophilic fluorination, polymer modification, and as a precursor for sulfonyl-based reagents, it is supplied in high-quality packaging to maintain stability and integrity. Store in a cool, dry place under inert conditions to preserve its reactivity.

CAS No: 1717-59-5
Molecular Formula: C2HF3O4S
Molecular Weight: 178.09
Exact Mass: 177.95476417
Monoisotopic Mass: 177.95476417
IUPAC Name: 2,2-difluoro-2-fluorosulfonylacetic acid
SMILES: C(=O)(C(F)(F)S(=O)(=O)F)O
Synonyms: 1717-59-5, 2,2-Difluoro-2-(fluorosulfonyl)acetic acid, DTXSID10372104, DTXCID70323137, 629-236-8

Application

2,2-Difluoro-2-(fluorosulfonyl)acetic acid is primarily used as a key intermediate in the synthesis of fluorinated organic compounds and sulfonyl derivatives. Its reactive fluorosulfonyl group enables applications in electrophilic fluorination reactions, which are critical in pharmaceutical and agrochemical research. Additionally, this compound serves as a precursor for advanced polymer modification and electrolyte additives in lithium-ion batteries. Researchers also utilize it in the development of novel surfactants and specialty chemicals due to its unique structural properties.

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