CAS 20621-29-8

Methanesulfinylchloride, 1,1,1-trifluoro-

Description:

Methanesulfinylchloride, 1,1,1-trifluoro- is a chemical compound characterized by its unique structure, which includes a sulfinyl group attached to a methane backbone and three fluorine atoms. This compound is typically a colorless to pale yellow liquid with a pungent odor, indicative of its reactivity and potential hazards. It is classified as a sulfonyl chloride, which makes it reactive towards nucleophiles, often participating in substitution reactions. The presence of trifluoromethyl groups enhances its electrophilicity, making it useful in various synthetic applications, particularly in the pharmaceutical and agrochemical industries. Due to its reactivity, it must 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. Its applications may include serving as an intermediate in the synthesis of more complex molecules, particularly those requiring sulfonyl functionalities.

Formula: F₃CSOCl

Synonyms:

• Methanesulfinylchloride, trifluoro-
• Perfluoromethanesulfinyl chloride
• Trifluoromethylsulfinyl chloride
• Trifluoromethane Sulfinyl Chloride
• 1,1,1-trifluoro-Methanesulfinylchloride
• rifluoromethanesulfinylchloride
• 1,1,1-Trifluoromethanesulfinyl chloride
• TrifluoroMethanesulfinyl chloride
• Methanesulfinylchloride, 1,1,1-trifluoro-
• TRIFLUOROMETHYL SULFINYL CHLORIDE
• trifluoromethyl sulfacyl chloride

Trifluoromethanesulfinyl chloride

CAS: 20621-29-8

Trifluoromethanesulfinyl chloride

Purity: 95%

Molecular weight: 152.52g/mol

Ref: 54-PC1002247

Trifluoromethylsulfinyl Chloride

Controlled Product

CAS: 20621-29-8

Formula: CClF₃OS

Color and Shape: Neat

Molecular weight: 152.523

Ref: TR-T791770

Trifluoromethanesulfinyl chloride

CAS: 20621-29-8

Trifluoromethanesulfinyl chloride is a reactive, asymmetric synthesis reagent that reacts with nucleophilic compounds to form the corresponding sulfinamides. Trifluoromethanesulfinyl chloride has been shown to react with amines to produce the corresponding sulfinamides in high yields. The chemical properties of this compound are similar to those of hydroxyl and hydroxy groups. Trifluoromethanesulfinyl chloride can be used as a hydrolysis agent for aliphatic hydrocarbons.br>br> The chemical formula for trifluoromethanesulfinyl chloride is CF3SO2Cl. It has a molecular mass of 217.24 g/mol and a boiling point of 211°C at atmospheric pressure. It is soluble in water, alcohols, ethers and acetone but insoluble in benzene, chloroform or carbon tetrachloride. This compound is reactive and should

Formula: CClF₃OS

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 152.52 g/mol

Ref: 3D-FT80952

Methanesulfinyl chloride, 1,1,1-trifluoro-

CAS: 20621-29-8

Formula: CClF₃OS

Purity: 95%

Color and Shape: Liquid

Molecular weight: 152.5233

Ref: IN-DA002IDM