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Phenylsulfenylchloride

CAS No.:
931-59-9
Catalog Number:
AG00GUHN
Molecular Formula:
C6H5ClS
Molecular Weight:
144.6219
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Product Description
Catalog Number:
AG00GUHN
Chemical Name:
Phenylsulfenylchloride
CAS Number:
931-59-9
Molecular Formula:
C6H5ClS
Molecular Weight:
144.6219
MDL Number:
MFCD11850482
IUPAC Name:
phenyl thiohypochlorite
InChI:
InChI=1S/C6H5ClS/c7-8-6-4-2-1-3-5-6/h1-5H
InChI Key:
JWUKZUIGOJBEPC-UHFFFAOYSA-N
SMILES:
ClSc1ccccc1
Properties
Complexity:
59.5  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
143.98g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
144.616g/mol
Monoisotopic Mass:
143.98g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
25.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.8  
Literature
Title Journal
Ti(IV)-catalyzed asymmetric sulfenylation of 1,3-dicarbonyl compounds. Chemistry (Weinheim an der Bergstrasse, Germany) 20070101
Intermolecular [4 + 2] cycloaddition of o-quinodimethanes derived from ene-bis(sulfinylallenes). The Journal of organic chemistry 20060901
Highly-functionalised difluorinated cyclohexane polyols via the Diels-Alder reaction: regiochemical control via the phenylsulfonyl group. Organic & biomolecular chemistry 20050921
Titanium(IV)-catalyzed enantioselective sulfenylation of beta-ketoesters. Organic letters 20050901
Reactions of methylenecyclopropanes with phenylsulfenyl chloride and phenylselenyl chloride. The Journal of organic chemistry 20040416
Sulfanyl- and selanyldifluoromethylphosphonates as a source of phosphonodifluoromethyl radicals and their addition onto alkenes. Organic letters 20010125
Properties