4237-48-3

Basic information

• Product Name: Benzenemethanethiol, alpha-phenyl-
• Synonyms: Benzenemethanethiol, alpha-phenyl-;benzhydryl hydrosulfide;Diphenylmethanethiol;α-Phenylbenzenemethanethiol;DiphenylMethanethiol, GC 97%;Benzophenone Mercaptan
• CAS NO: 4237-48-3
• Molecular Formula: C₁₃H₁₂S
• Molecular Weight: 200.2994
• Mol File: 4237-48-3.mol
• Article Data: 19

Chemical Properties

• Boiling Point: 310.2°Cat760mmHg
• Flash Point: 125.8°C
• Appearance: /
• Density: 1.09g/cm³
• Vapor Pressure: 0.00111mmHg at 25°C
• Refractive Index: 1.607
• PKA: 9.27±0.10(Predicted)
• CAS DataBase Reference: Benzenemethanethiol, alpha-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanethiol, alpha-phenyl-(4237-48-3)
• EPA Substance Registry System: Benzenemethanethiol, alpha-phenyl-(4237-48-3)

Safety Data

• Hazardous Substances Data: 4237-48-3(Hazardous Substances Data)

Usage

Uses

Diphenylmethanethiol can be used as a reactant and a catalyst.

InChI:InChI=1/C13H12S/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H

Upstream product

• 91-01-0 1,1-Diphenylmethanol 
• 952-92-1 1-Benzyl-1,4-dihydronicotinamide 
• 64-17-5 ethanol 
• 1450-31-3 Thiobenzophenon 
• 861547-85-5 benzhydrylmercaptocarbonylmercapto-acetic acid 
• 861578-40-7 dithiocarbonic acid S,S'-dibenzhydryl ester 
• 17356-08-0 thiourea 
• 90-99-3 diphenylchloromethane 
• 908093-98-1 diazodiphenylmethane 
• 464-72-2 tetraphenylethane-1,2-diol 
• 93551-90-7 N-Phenylbenzhydrylmonothiocarbamate 
• 93551-89-4 S-benzhydryl N-phenylthiocarbamate 
• 709-82-0 diphenylmethinium 
• 53392-47-5 diphenylmethyl thioacetate 

Downstream Products

• 52752-79-1 benzhydryl-isopropyl sulfone 
• 7327-11-9 1-(2-benzhydrylmercapto-ethyl)-piperidine 
• 6974-50-1 diphenylmethyl ethyl sulfone 
• 93727-95-8 1-ethoxy-2-diphenylmethanesulfonyl-ethane 
• 122725-11-5 dibenzhydryl trisulfide 
• 21367-78-2 dibenzhydryl tetrasulfide 
• 1726-02-9 bis(diphenylmethyl)disulfide 
• 111499-71-9 4-nitro-thiobenzoic acid S-benzhydryl ester 
• 72250-70-5 benzhydryl-propyl sulfone 
• 874506-46-4 benzhydryl-(2-chloro-ethyl)-sulfone 
• 874506-41-9 benzhydryl-(3-chloro-propyl)-sulfone 
• 1726-03-0 diphenylmethyl sulfide 
• 94001-59-9 2-benzhydrylsulfanyl ethanol 
• 95742-42-0 2-diphenylmethanesulfonyl-ethanol 

Relevant articles and documents

The unusual influence of hetaryl groups on the direct conversion of some secondary alcohols into thiols with Lawesson’s reagent: elucidation of the reaction mechanism

A series of hetaryl-substituted methanols were used for direct conversion into the corresponding thiols by treatment with Lawesson’s reagent in boiling toluene. Unexpectedly, the respective sulfides were formed exclusively. In the case of chiral alcohols,

HETEROCYCLIC COMPOUNDS WITH WORKING MEMORY ENHANCING ACTIVITY

The present invention relates to a chemical compound having the general formula (I): wherein R1 and R2 are, equal or independently, aryl, heteroaryl; wherein RTA is a 2-1,3-, or 4- 1,3- or 5-1,3-thiazole ring and its use in for improving; the short term memory and/or the working memory.

Synthesis and structure of dinitrosyl iron complexes with secondary thiolate bridging ligands [Fe2(μ-SCHR2)2(NO)4], R = Me, Ph

New dinitrosyl iron complexes of binuclear structure [Fe2(μ-SCHMe2)2(NO)4] and [Fe2(μ-SCHPh2)2(NO)4] were first synthesized employing new method from Fe(CO)5, corresponding thiol, and EtONO. Complexes structures were determined by XRD technique. DFT calculations were performed to probe the cis-conformer structures in gas and solution phases. NO donor ability of the complex with isopropyl thiolate ligand was studied.