83711-12-0

Basic information

• Product Name: 5,5-bis(phenylthio)-1-pentanol
• Synonyms: 5,5-bis(phenylthio)-1-pentanol
• CAS NO: 83711-12-0
• Molecular Weight: 304.477
• Mol File: 83711-12-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 5,5-bis(phenylthio)-1-pentanol(CAS DataBase Reference)
• NIST Chemistry Reference: 5,5-bis(phenylthio)-1-pentanol(83711-12-0)
• EPA Substance Registry System: 5,5-bis(phenylthio)-1-pentanol(83711-12-0)

Safety Data

• Hazardous Substances Data: 83711-12-0(Hazardous Substances Data)

Upstream product

• 109-99-9 tetrahydrofuran 
• 13307-76-1 [bis(phenylthio)methyl]lithium 
• 1191-99-7 2,3-dihydro-2H-furan 
• 108-98-5 thiophenol 
• 1927-61-3 2-(2-phenylethoxy)tetrahydro-2H-pyran 
• 110-87-2 3,4-dihydro-2H-pyran 

Downstream Products

• 65756-04-9 trans-(±)-2-(phenylthio)cyclopentanol 
• 78086-89-2 cis-2-(Phenylthio)cyclopentanol 
• 83711-13-1 5,5-bis(phenylthio)-1-pentyl benzenesulfonate 
• 263565-59-9 5,5-bis(phenylthio)pentyl benzoate 
• 263565-65-7 5,5-bis(phenylthio)pentyl octanoate 
• 263565-64-6 5,5-bis(phenylthio)pentyl 3-phenylpropanoate 
• 83711-10-8 1,1-bis(phenylthio)-6,6-bis-((p-tertbutylphenyl)thio)hexane 
• 83711-20-0 5-iodo-1,1-bis(phenylthio)pentane 
• 83711-04-0 6,6-bis(phenylthio)bicyclo<3.1.0>hexane 

Relevant articles and documents

Ring Opening Alkylation of Tetrahydrofuran with Some Heterosubstituted Organolithium Reagents by the Aid of Boron Trifluoride Etherate

Organolithium reagents stabilized by halogeno, thio, silyl, vinyl and/or phenyl substituent(s) can cleave THF effectively under the influence of boron trifluoride etherate at lower temperatures.The softness of these carbanionic reagents seems to be import

Catalyst-dependent selective synthesis of O/S- and S/S-acetals from enol ethers

Enol ethers are reacted with mercaptanes to give the corresponding O/S- or S/S-acetals in medium to high yield. Either product can be formed selectively depending on the acid catalyst and the reaction time applied.

MONOTHIOACETALIZATION OF ACETALS USING DIETHYLALUMINIUM THIOPHENOXIDE

Reactions of diethylaluminium thiophenoxide (Et2AlSPh) with acetals of several types, in which acyclic, cyclic, and bicyclic ones are involved, were examined in comparison with the known reaction using thiophenol in the presence of Lewis acid and found to provide a new and efficient method for preparation of monothioacetals.