99689-27-7

Basic information

• Product Name: dicyclohexyl(phenyl)phosphine sulfide
• Synonyms: dicyclohexyl(phenyl)phosphine sulfide
• CAS NO: 99689-27-7
• Molecular Weight: 306.452
• Mol File: 99689-27-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: dicyclohexyl(phenyl)phosphine sulfide(CAS DataBase Reference)
• NIST Chemistry Reference: dicyclohexyl(phenyl)phosphine sulfide(99689-27-7)
• EPA Substance Registry System: dicyclohexyl(phenyl)phosphine sulfide(99689-27-7)

Safety Data

• Hazardous Substances Data: 99689-27-7(Hazardous Substances Data)

Upstream product

• 644-97-3 Dichlorophenylphosphine 
• 591-50-4 iodobenzene 
• 6476-37-5 dicyclohexylphenylphosphine 
• 16523-54-9 chlorodicyclohexylphosphane 

Downstream Products

• 1621088-52-5 (Z)-dicyclohexyl(2-styrylphenyl)phosphine sulfide 
• 1621088-14-9 (E)-dicyclohexyl(2-styrylphenyl)phosphine sulfide 
• 1621088-44-5 (E)-(2-(6-chloro-1-phenylhex-1-en-2-yl)phenyl)dicyclohexylphosphine sulfide 
• 1621088-62-7 (Z)-(2-(6-chloro-1-phenylhex-1-en-2-yl)phenyl)dicyclohexylphosphine sulfide 
• 1621088-42-3 (E)-dicyclohexyl(2-(1-phenylhex-1-en-2-yl)phenyl)phosphine sulfide 
• 1621088-38-7 (E)-dicyclohexyl(2-(1,2-di-p-tolylvinyl)phenyl)phosphine sulfide 
• 1621088-40-1 (Z)-dicyclohexyl(2-(1,2-di-p-tolylvinyl)phenyl)phosphine sulfide 
• 1621088-34-3 (E)-(2-(1,2-bis(4-methoxyphenyl)vinyl)phenyl)dicyclohexylphosphine sulfide 
• 1621088-36-5 (Z)-(2-(1,2-bis(4-methoxyphenyl)vinyl)phenyl)dicyclohexylphosphine sulfide 
• 1621088-32-1 (E)-(2-(1,2-bis(4-chlorophenyl)vinyl)phenyl)dicyclohexylphosphine sulfide 
• 1621088-30-9 (E)-dicyclohexyl (2-(1,2-diphenylvinyl)phenyl)phosphine sulfide 
• 1621087-92-0 (E)-dicyclohexyl (2-(1-phenylprop-1-en-2-yl)phenyl)phosphine sulfide 
• 1621088-12-7 (E)-3-(2-(dicyclohexylphosphorothioyl)phenyl)-N,N-dimethylacrylamide 
• 1621088-13-8 (Z)-3-(2-(dicyclohexylphosphorothioyl)phenyl)-N,N-dimethylacrylamide 

Relevant articles and documents

Radical phosphination of organic halides and alkyl imidazole-1- carbothioates

Taking advantage of a radical-based methodology, mild and chemoselective phosphination reactions of organic halide and alkyl imidazole-1-carbothioates have been developed. The mild reaction conditions allow labile functional groups to survive during the reaction. Copyright