3462-50-8

Basic information

• Product Name: Benzene, 1,1'-[(1-phenylethylidene)bis(thio)]bis-
• CAS NO: 3462-50-8
• Molecular Formula: C20H18S2
• Molecular Weight: 322.495
• Mol File: 3462-50-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-[(1-phenylethylidene)bis(thio)]bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-[(1-phenylethylidene)bis(thio)]bis-(3462-50-8)
• EPA Substance Registry System: Benzene, 1,1'-[(1-phenylethylidene)bis(thio)]bis-(3462-50-8)

Safety Data

• Hazardous Substances Data: 3462-50-8(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 492-37-5 hydratropic acid 
• 882-33-7 diphenyldisulfane 
• 536-74-3 phenylacetylene 
• 16336-45-1 α-phenylthiostyrene 
• 4316-37-4 1,1,-diethoxy-1-phenylethane 
• 4551-15-9 phenylthiotrimethylsilane 
• 3674-77-9 2-methyl-2-phenyl-1,3-dioxolane 
• 98-86-2 acetophenone 

Downstream Products

• 134896-73-4 6-phenyl-6-phenylthio-1-heptene 
• 56399-58-7 rel(1R,2S)-1,2-dimethyl-1-phenyl cyclopentane 
• 56399-58-7 rel(1R,2S)-1,2-dimethyl-1-phenyl cyclopentane 
• 1677-87-8 acetophenone 2,4-dinitrophenylhydrazone 
• 833-81-8 (E)-1,2-diphenylpropene 
• 833-81-8 1,2-diphenylpropene 
• 4148-93-0 2-phenyl-2-propyl phenyl sulfide 
• 16336-45-1 α-phenylthiostyrene 
• 121410-58-0 C₁₇H₁₈S 
• 104367-37-5 2-Phenyl-2-phenylsulfanyl-pentan-3-ol 
• 104367-36-4 1,2-Diphenyl-2-phenylsulfanyl-propan-1-ol 
• 104367-39-7 C₂₁H₂₀S 
• 98-86-2 acetophenone 
• 40390-78-1 [(1-phenylethyl)thio]benzene 

Relevant articles and documents

λ3-Iodanes as Visible Light Photocatalyst in Thioacetalization of Aldehydes

Introduction of an iodine(III) reagent as visible-light photocatalyst for chemoselective dithioacetalization has been the limelight of the current methodology. The mechanistic investigations reveal that the reactions proceeded via radical pathway upon lig

Highly regioselective double hydrothiolation of terminal acetylenes with thiols catalyzed by palladium diacetate

Treatment of terminal acetylenes 1 with two equivalents of thiols 2 in the presence of Pd(OAc)2 catalyst and H2O causes regioselective double hydrothiolation of 1, leading to the corresponding dithioketals 3 in moderate to good yields.

Green, catalyst-free thioacetalization of carbonyl compounds using glycerol as recyclable solvent

We describe herein the use of glycerol as an efficient and a recyclable solvent in the thioacetalization of aldehydes and ketones. The catalyst-free reactions proceed easily using glycerol at 90 °C and the corresponding thioacetals were obtained in good to excellent yields. Glycerol was recovered and utilized for further thioacetalization reactions.