CAS 91183-99-2

2,2,2-Trifluoroethanesulfinyl chloride

Description:

2,2,2-Trifluoroethanesulfinyl chloride is a chemical compound characterized by its sulfinyl functional group and the presence of trifluoromethyl groups. It is typically a colorless to pale yellow liquid with a pungent odor, indicative of its reactivity and potential hazards. The compound is known for its role as a reagent in organic synthesis, particularly in the introduction of sulfinyl groups into various organic molecules. Its trifluoromethyl groups contribute to its unique electronic properties, enhancing its reactivity and making it useful in various chemical transformations. The presence of chlorine in its structure also suggests that it can participate in nucleophilic substitution reactions. Due to its reactivity, 2,2,2-Trifluoroethanesulfinyl chloride should be handled with care, as it can be corrosive and may pose health risks upon exposure. Proper safety measures, including the use of personal protective equipment and working in a well-ventilated area or fume hood, are essential when working with this compound.

Formula: C₂H₂ClF₃OS

InChI: InChI=1S/C2H2ClF3OS/c3-8(7)1-2(4,5)6/h1H2

InChI key: InChIKey=NTOLLMQTDUCPKD-UHFFFAOYSA-N

SMILES: C(C(F)(F)F)S(Cl)=O

Synonyms:

• 2,2,2-Trifluoroethanesulfinyl chloride
• 2,2,2-Trifluoroethane-1-sulfinyl chloride
• Ethanesulfinyl chloride, 2,2,2-trifluoro-

2,2,2-Trifluoroethanesulfinyl chloride

CAS: 91183-99-2

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Formula: C₂H₂ClF₃OS

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 166.55 g/mol

Ref: 3D-RDA18399