CAS 594-42-3
:Trichloromethanesulfenyl chloride
Description:
Trichloromethanesulfenyl chloride, also known as chlorothioformyl chloride, is a chemical compound characterized by its unique structure and reactivity. It features a trichloromethyl group attached to a sulfenyl chloride functional group, making it a potent electrophile. This compound is typically a colorless to pale yellow liquid with a pungent odor, indicative of its reactivity and potential hazards. It is soluble in organic solvents but reacts with water, releasing hydrochloric acid and producing sulfur-containing byproducts. Trichloromethanesulfenyl chloride is primarily used in organic synthesis, particularly in the preparation of thioesters and other sulfur-containing compounds. Due to its reactivity, it must be handled with care, as it can be corrosive and harmful 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 in chemical synthesis highlight its importance in the field of organic chemistry.
Formula:CCl4S
InChI:InChI=1S/CCl4S/c2-1(3,4)6-5
InChI key:InChIKey=RYFZYYUIAZYQLC-UHFFFAOYSA-N
SMILES:C(SCl)(Cl)(Cl)Cl
Synonyms:- (Trichloromethyl)sulfenyl chloride
- Excessive Chlorine Methyl Mercaptan
- High Chloride Methyl Mercaptan
- Methanesulfenyl chloride, trichloro-
- NSC 66404
- Perchloromethanethiol
- Perchloromethyl mercaptan
- Tetrachloro Methyl Mercaptan
- Tetrachloro-Sulfur Carbonyl
- Trichloromethanesulfenyl chloride
- Trichloromethanesulphenyl chloride
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