ChemicalBook--->CAS DataBase List--->931-59-9

931-59-9

931-59-9 Structure

931-59-9 Structure
IdentificationBack Directory
[Name]

Phenylsulfenylchloride
[CAS]

931-59-9
[Synonyms]

fenyL
(Chlorothio)benzene
Phenylthio chloride
Phenylchloro sulfide
Phenylsulfenylchloride
Benzene, (chlorothio)-
(Chlorosulfanyl)benzene
Phenyl Thiohypochlorite
BENZENESULFENYL CHLORIDE
Phenylsulphenyl chloride
phenyl hypochlorothioite
BenzeneSulfenic acid chloride
Phenylsulfenylchloride ISO 9001:2015 REACH
[EINECS(EC#)]

632-987-4
[Molecular Formula]

C6H5ClS
[MDL Number]

MFCD11850482
[MOL File]

931-59-9.mol
[Molecular Weight]

144.622
Chemical PropertiesBack Directory
[Boiling point ]

262℃
[density ]

1.25
[Fp ]

110℃
Questions And Answer(Q&A)Back Directory
[Preparation]

To a flask containing 32.7 gm (0.15 mole) of diphenyl disulfide dissolved in 100 ml of dichloromethane containing 3 ml of pyridine is slowly dropwise added at room temperature 20.3 gm (0.15 mole) of freshly distilled sulfuryl chloride. After completion of the addition, the solution is stirred for an additional hour, concentrated under reduced pressure (12 mm Hg) at 25°C, and the residue distilled to afford 33 gm (76%), b.p. 49°C (4 mm Hg), of a dark red liquid.
Preparation of Benzenesulfenyl Chloride
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H315
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Benzene,1-methoxy-4-(phenylthio)--->4-PHENYLTHIOPHENOL-->S-PHENYL THIOACETATE-->Phenol-->Acetyl chloride-->DIPHENYL DISULFIDE
[Preparation Products]

1-(phenylthio)pyrrolidine-2,5-dione-->Benzene, (1-chloroethoxy)--->N-TERT-BUTYLBENZENESULFENAMIDE-->4-tert-Butyldiphenyl sulfide-->4-METHYLBENZANILIDE-->BENZANILIDE
Hazard InformationBack Directory
[Uses]

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.
[Synthesis Reference(s)]

The Journal of Organic Chemistry, 43, p. 1208, 1978 DOI: 10.1021/jo00400a041
Chemical and Pharmaceutical Bulletin, 28, p. 126, 1980 DOI: 10.1248/cpb.28.126
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