37457-08-2

Basic information

• Product Name: Benzene, 1,1'-[cyclohexylidenebis(thio)]bis-
• CAS NO: 37457-08-2
• Molecular Formula: C18H20S2
• Molecular Weight: 300.489
• Mol File: 37457-08-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-[cyclohexylidenebis(thio)]bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-[cyclohexylidenebis(thio)]bis-(37457-08-2)
• EPA Substance Registry System: Benzene, 1,1'-[cyclohexylidenebis(thio)]bis-(37457-08-2)

Safety Data

• Hazardous Substances Data: 37457-08-2(Hazardous Substances Data)

Upstream product

• 108-94-1 cyclohexanone 
• 882-33-7 diphenyldisulfane 
• 4922-47-8 1-(phenylthio)cyclohex-1-ene 
• 4551-15-9 phenylthiotrimethylsilane 
• 931-57-7 1-methoxy-cyclohex-1-ene 
• 108-98-5 thiophenol 
• 110452-14-7 2-phenylthiocyclohexanone 
• 822-87-7 2-Chlorocyclohexanone 
• 177-15-1 1-oxa-4-thia-spiro[4.5]decane 
• 177-10-6 1,3-dioxolane-2-spirocyclohexane 
• 933-40-4 cycloxexanone dimethyl ketal 

Downstream Products

• 1589-62-4 cyclohexanone (2,4-dinitrophenyl)hydrazone 
• 85894-96-8 dimethyl (2-(phenylthio)-1-cyclohexen-3-yl)malonate 
• 85894-97-9 methyl 2-(2-(phenylthio)-1-cyclohexen-3-yl)-3-oxobutyrate 
• 85895-11-0 2-(phenylthio)-3-(phenylethynyl)-1-cyclohexene 
• 85894-93-5 6-bromo-1-(phenylthio)cyclohexene 
• 85894-92-4 1-(phenylthio)-2-bromocyclohexene 
• 85894-85-5 6-methyl-1-cyclohexenyl phenyl sulfide 
• 63965-89-9 dimethyl 2-(2-oxocyclohexyl)malonate 
• 71634-05-4 3-phenyl-2-(phenylthio)cyclohexene 
• 1886-64-2 3,3-dimethylbut-1-en-2-yl phenyl sulfide 
• 4922-47-8 1-(phenylthio)cyclohex-1-ene 
• 115993-77-6 1-(phenylthio)-1-(2-propenyl)cyclohexane 
• 89423-43-8 (1-Chloro-cyclohexylsulfanyl)-benzene 
• 882-33-7 diphenyldisulfane 

Relevant articles and documents

2,4,6-Trichloro-1,3,5-triazine catalyzed chemoselective transthioacetalization of aldehyde acetals and oxathioacetals

A mild and efficient transthioacetalization of aldehyde acetals and oxathioacetals was carried out using 2,4,6-trichloro-1,3,5-triazine as a mild and inexpensive catalyst. Chemoselective transacetalization is impressive as aldehyde O,O- and O,S-acetals ar

Unprecedented polymer-supported π-acid: Synthesis and its application as a promoter to the monothioacetalization of acetals

A novel polymer was synthesized by copolymerization of styrene monomer bearing dicyanoketene acetal functionality and ethylene glycol dimethacrylate, and used successfully as a recyclable π-acid catalyst in monothioacetalization of aromatic, aliphatic, acyclic, and cyclic acetals with thiophenol and phenylthiotrimethylsilane.

A Convenient Method for the Transformation of Alkenyl Sulfides to 2-(Phenylthio)alkanenitriles, Homoallyl Sulfides, and Thioacetals

2-(Phenylthio)alkanenitriles, homoallyl sulfides, and thioacetals were obtained in good yields by the reaction of alkenyl sulfides with the corresponding silyl nucleophiles via thionium ion intermediates.