7315-50-6

Basic information

• Product Name: Benzene, [bis(butylthio)methyl]-
• CAS NO: 7315-50-6
• Molecular Formula: C15H24S2
• Molecular Weight: 268.488
• Mol File: 7315-50-6.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzene, [bis(butylthio)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [bis(butylthio)methyl]-(7315-50-6)
• EPA Substance Registry System: Benzene, [bis(butylthio)methyl]-(7315-50-6)

Safety Data

• Hazardous Substances Data: 7315-50-6(Hazardous Substances Data)

Upstream product

• 109-79-5 n-butanethiol 
• 100-52-7 benzaldehyde 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 772-01-0 2-phenyl-1,3-dioxane 
• 123290-13-1 phenyltriisopropylsilylmethanone 
• 132868-67-8 (tert-butyldimethylsilyl)(phenyl)methanone 
• 63935-93-3 benzoyltriethylsilane 
• 20025-27-8 β-phenylvinyl butyl sulfide 
• 936-51-6 2-phenyl-1,3-dioxolane 
• 6425-08-7 4,4'-(phenylmethylene)bismorpholine 

Downstream Products

• 629-45-8 dibutyl disulfide 
• 100-52-7 benzaldehyde 
• 77953-85-6 bis-(butane-1-sulfonyl)-phenyl-methane 

Relevant articles and documents

Direct anodic (thio)acetalization of aldehydes with alcohols (thiols) under neutral conditions, and computational insight into the electrochemical formation of the acetals

A versatile protocol for the production of acetals/thioacetals by means of direct electrochemical oxidation is developed here under neutral conditions, providing (thio)acetals with good functional group tolerance and a wide scope for both aldehydes and (thio)alcohols. DFT calculations reveal that direct electron transfer from the anode plays a key role in carbonyl activation during this acid free acetalization process.

Silicon benzoyl a method for preparing benzaldehyde thio-acetal

The invention provides a method for preparing benzaldehyde sulfo-acetal through benzaldehyde silicon, and relates to the field of preparation of sulfur compounds and silicon compounds. The benzaldehyde silicon and alkyl sulfhydryl (including primary merca

Heteropoly acids as heterogeneous catalysts for thioacetalization and transthioacetalization reactions

Heteropoly acids are effective solid catalysts for the thioacetalization of carbonyl compounds. Tungstophosphoric acid (H3PW12O40), was found to be an effective and a highly selective catalyst for the thioacetalization of aldehydes, ketones and for the transthioacetalization of acetals, acylals and O,S-acetals which proceeded in excellent yields in the absence of solvent. The catalyst has also been successfully applied to the chemoselective conversion of α- or β-diketones and a β-keto ester into the corresponding dithioacetals. Sterically hindered carbonyl compounds such as camphor and benzophenone were also converted to their corresponding thioacetals in refluxing petroleum ether in 89-94percent yields. Surprisingly, anthrone was reduced to anthracene in 91percent yield.