CAS 931-59-9
:Benzenesulfenyl chloride
Description:
Benzenesulfenyl chloride, with the CAS number 931-59-9, is an organosulfur compound characterized by the presence of a sulfenyl chloride functional group attached to a benzene ring. It appears as a colorless to pale yellow liquid and has a pungent odor. This compound is known for its reactivity, particularly in nucleophilic substitution reactions, where it can act as a sulfenylating agent, introducing a sulfenyl group into various substrates. Benzenesulfenyl chloride is soluble in organic solvents such as dichloromethane and ether but is generally insoluble in water due to its hydrophobic benzene structure. It is sensitive to moisture and can hydrolyze to form benzenesulfenic acid, which is less stable. Safety precautions are essential when handling this compound, as it can be corrosive and irritating to the skin, eyes, and respiratory system. Proper storage in a cool, dry place away from moisture is recommended to maintain its stability and reactivity.
Formula:C6H5ClS
InChI:InChI=1S/C6H5ClS/c7-8-6-4-2-1-3-5-6/h1-5H
InChI key:InChIKey=JWUKZUIGOJBEPC-UHFFFAOYSA-N
SMILES:S(Cl)C1=CC=CC=C1
Synonyms:- (Chlorosulfanyl)benzene
- (Chlorothio)benzene
- Benzene, (chlorothio)-
- Hypochlorothioous acid, phenyl ester
- Phenyl chloro sulfide
- Phenylsulfenyl chloride
- Phenylsulphenyl chloride
- Benzenesulfenyl chloride
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Found 2 products.
Phenylsulfenyl Chloride
CAS:Controlled ProductApplications Phenylsulfenyl Chloride is an intermediate used in the synthesis of Tabanone (T003450), which is found in oils of Trifolium pratense L. and is a potential natural anti-oxidant.
References Vlaisavljevic, S., et. al.: Molecules, 19, 713 (2014)Formula:C6H5ClSColor and Shape:NeatMolecular weight:144.622
