1854-83-7

Basic information

• Product Name: α-(4-Chlor-benzol-sulfonyl)-styrol
• Synonyms: α-(4-Chlor-benzol-sulfonyl)-styrol
• CAS NO: 1854-83-7
• Molecular Weight: 278.759
• Mol File: 1854-83-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: α-(4-Chlor-benzol-sulfonyl)-styrol(CAS DataBase Reference)
• NIST Chemistry Reference: α-(4-Chlor-benzol-sulfonyl)-styrol(1854-83-7)
• EPA Substance Registry System: α-(4-Chlor-benzol-sulfonyl)-styrol(1854-83-7)

Safety Data

• Hazardous Substances Data: 1854-83-7(Hazardous Substances Data)

Upstream product

• 106-54-7 p-Chlorothiophenol 
• 140-10-3 (E)-3-phenylacrylic acid 
• 14752-66-0 sodium p-chlorobenzenesulphinate 
• 100-42-5 styrene 
• 673-41-6 p-chlorobenzenediazonium tetrafluoroborate 
• 96-09-3 styrene oxide 
• 3405-89-8 2-(4-chloro-phenylsulfonyl)acetic acid 
• 100-52-7 benzaldehyde 
• 1854-84-8 1-chloro-4-((2-chloro-2-phenylethyl)sulfonyl)benzene 

Downstream Products

• 40582-90-9 p-chlorophenyl 2-phenylhexyl sulfone 
• 40582-89-6 p-Chlorphenyl-2-phenylpropyl-sulfon 
• 51118-27-5 1-benzyl-5-phenyl-1H-1,2,3-triazole 
• 2034-28-8 1-(4-methoxyphenyl)-5-phenyl-1H-[1,2,3]-triazole 
• 4874-85-5 1,5-diphenyl-1H-1,2,3-triazole 
• 1009089-58-0 1-octyl-5-phenyl-1H-[1,2,3]triazole 
• 51720-16-2 1-<(carboethoxy)-methyl>-5-phenyl-1H-1,2,3-triazole 
• 1097725-23-9 methyl 4-(4-chlorophenylsulfonyl)-3-phenylbutyrate 
• 6031-02-3 2-phenylhexane 

Relevant articles and documents

1,5-disubstituted 1,2,3-triazolylation at C1, C2, C3, C4, and C6 of pyranosides: A metal-free route to triazolylated monosaccharides and triazole-linked disaccharides

A pair of easily accessible vinyl sulfones derived from styrene epoxide and monotosylated glycerol were reacted with six different azidopyranosides having an azido group at C1, C2, C3, C4, C6, and at the terminal position of an exocylic chain attached to

An efficient one-pot, three-component synthesis of vinyl sulfones via iodide-catalyzed radical alkenylation

An efficient one-pot, three-component synthesis of vinyl sulfones via iodide-catalyzed radical alkenylation using aryl diazonium salts, terminal alkenes and DABSO is reported. This protocol offers good yields and tolerates a broad range of functional groups. Based on the extensive control experiments, we propose a plausible radical mechanism.