25636-61-7

Basic information

• Product Name: 2-phenyl-1,3-propanedithiol
• Synonyms: 2-phenyl-1,3-propanedithiol
• CAS NO: 25636-61-7
• Molecular Weight: 184.326
• Mol File: 25636-61-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-phenyl-1,3-propanedithiol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-1,3-propanedithiol(25636-61-7)
• EPA Substance Registry System: 2-phenyl-1,3-propanedithiol(25636-61-7)

Safety Data

• Hazardous Substances Data: 25636-61-7(Hazardous Substances Data)

Upstream product

• 6133-92-2 4-Phenyl-1,2-dithiolane 
• 1159-54-2 tri(4-chlorophenyl)phosphine 
• 1570-95-2 2-phenylpropane-1, 3-diol 
• 64923-68-8 2-phenylpropane-1,3-diyl dimethanesulfonate 
• 83-13-6 diethyl 2-phenylmalonate 
• 1570-96-3 2-Phenyl-1,3-propandiol-di-p-toluolsulfonsaeureester 

Downstream Products

• 1397685-18-5 5-phenyl-1,3-dithiane 
• 1461660-71-8 2-(4-methoxyphenyl)-5-phenyl-1,3-dithiane 
• 6133-92-2 4-Phenyl-1,2-dithiolane 

Relevant articles and documents

Facile deprotection of dithioacetals by using a novel 1,4-benzoquinone/cat. NaI system

The combination of 1,4-benzoquinone and a catalytic amount of NaI was found to be effective for the deprotection of dithioacetals. The reactions proceeded efficiently under mild, near-neutral reaction conditions, producing a wide range of aryl and alkyl aldehydes and ketones generally in high yields with good functional group compatibility. The method developed therefore represents a general, facile, and highly applicable approach for deprotecting dithioacetals.

THE REDUCTION OF CYCLIC DISULPHIDES WITH TRIARYLPHOSPHINES IN AQUEOUS ORGANIC SOLVENTS

The kinetics of the reduction of cyclic disulphides with triphenylphosphine have been studied in aqueous ethanol at various temperatures.Solvent effects on the reaction of 4-phenyl-1,2-dithiolane with tris-(4-chlorophenyl) phosphine in a number of aqueous organic solvents have been analysed in terms of the Kirkwood, Y and ENT functions.