67207-21-0

Basic information

• Product Name: Benzenesulfenyl bromide, 4-chloro-
• CAS NO: 67207-21-0
• Molecular Formula: C6H4BrClS
• Molecular Weight: 223.521
• Mol File: 67207-21-0.mol

Chemical Properties

• CAS DataBase Reference: Benzenesulfenyl bromide, 4-chloro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfenyl bromide, 4-chloro-(67207-21-0)
• EPA Substance Registry System: Benzenesulfenyl bromide, 4-chloro-(67207-21-0)

Safety Data

• Hazardous Substances Data: 67207-21-0(Hazardous Substances Data)

Upstream product

• 68360-42-9 1-chloro-4-phenoxymethylsulfanyl-benzene 
• 1146-44-7 4,4'-dichlorophenyl thiosulfonate 
• 83767-73-1 (bromomethyl)(4-chlorophenyl)sulfane 
• 1142-19-4 4,4'-dichlorodiphenyl disulfide 

Downstream Products

• 14204-31-0 2-(4-chlorophenylthio)isoindoline-1,3-dione 
• 38307-70-9 1-Brom-2-(p-chlorphenylthio)propan 

Relevant articles and documents

Design, synthesis and biological evaluation of sulfenimine cephalosporin sulfoxides as β-lactamase inhibitors

Abstract A series of sulfenimine cephalosporin sulfoxide derivatives (7a-v) were designed, synthesized and evaluated for their inhibitory activity against TEM-1 and cephalosporinase in cell-free systems. Some of the tested compounds showed enhanced inhibi

Synthesis of α-Haloalkyl Aryl Ethers from O,S-Acetals

α-Haloalkyl aryl ethers are prepared under mild conditions in high yileds by selective cleavage of O,S-acetals using sulfuryl chloride or bromine.The intermediate O,S-acetal is prepared from the phenol by O-alkylation using a readily accessible α-haloalkyl thioether.

SULFENYL CHLORIDES, XIV; THE REACTION OF ARYLTHIOSULFONATES WITH ARYLSULFENYL HALIDES

Utilizing partial results published earlier , the sulfenylation reaction of aromatic thiolsulfonates was investigated.Aromatic thiolsulfonates rapidly react with sulfenyl bromide in acetonitrile solution, whereas with sulfenyl chloride the splitting of the thiolsulfonate bond proceeds only in dimethylformamide and under forceful conditions.