64269-39-2

Basic information

• Product Name: Benzene, 1,1'-[butylidenebis(thio)]bis-
• CAS NO: 64269-39-2
• Molecular Formula: C16H18S2
• Molecular Weight: 274.451
• Mol File: 64269-39-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-[butylidenebis(thio)]bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-[butylidenebis(thio)]bis-(64269-39-2)
• EPA Substance Registry System: Benzene, 1,1'-[butylidenebis(thio)]bis-(64269-39-2)

Safety Data

• Hazardous Substances Data: 64269-39-2(Hazardous Substances Data)

Upstream product

• 123-72-8 butyraldehyde 
• 108-98-5 thiophenol 
• 882-33-7 diphenyldisulfane 

Downstream Products

• 121410-49-9 (1-Propyl-2-vinyl-pentylsulfanyl)-benzene 
• 121410-50-2 (3-Methyl-1-propyl-2-vinyl-pentylsulfanyl)-benzene 
• 1126-80-3 (n-butylthio)benzene 
• 128098-99-7 methyl (2RS,3RS)-2,3-dimethyl-4,4-bis(phenylthio)heptanoate 
• 128098-70-4 (2S,3R)-3-Methyl-2,4,4-tris-phenylsulfanyl-heptanoic acid methyl ester 
• 128098-70-4 methyl (2RS,3RS)-3-methyl-2,4,4-tris(phenylthio)heptanoate 
• 78427-96-0 1-phenyloctan-4-one 
• 128099-25-2 C₂₇H₃₀S₃ 
• 128099-25-2 C₂₇H₃₀S₃ 
• 128099-22-9 4-methyl-3,5,5-tris(phenylthio)octan-2-ol 
• 128099-14-9 3-methyl-2,4,4-tris(phenylthio)heptanal 
• 76200-43-6 (1-Benzenesulfinyl-butyl)-trimethyl-silane 
• 128098-87-3 (Z)-(5RS,6RS)-5,7-dimethyl-4,6,7-tris(phenylthio)oct-2-ene 
• 128098-87-3 (E)-(5RS,6RS)-5,7-dimethyl-4,6,7-tris(phenylthio)oct-2-ene 

Relevant articles and documents

Ethyl lactate mediated thioacetalization of aldehydes at ambient temperature

Dithioacetalization reactions of aldehydes with thiols/thiophenols have been successfully achieved at room temperature by employing the green, bio-based ethyl lactate as the reaction medium. By means of this sustainable approach, a class of dithioacetals has been acquired with high diversity and efficiency.

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.

Selenonium ionic liquid as an efficient catalyst for the synthesis of thioacetals under solvent-free conditions

Acidic ionic liquid butyl ethyl phenyl selenonium tetrafluoroborate, [BEPSe]BF4, was successfully employed as a catalyst for the synthesis of several dithioacetals in the absence of a solvent. The method is general and selectively afforded thioacetals derived from aldehydes and ketones in good yields.