2408-08-4

Basic information

• Product Name: (3-fluorobenzyl)(trifluoromethyl)sulfane
• Synonyms: (3-fluorobenzyl)(trifluoromethyl)sulfane
• CAS NO: 2408-08-4
• Molecular Weight: 210.195
• Mol File: 2408-08-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (3-fluorobenzyl)(trifluoromethyl)sulfane(CAS DataBase Reference)
• NIST Chemistry Reference: (3-fluorobenzyl)(trifluoromethyl)sulfane(2408-08-4)
• EPA Substance Registry System: (3-fluorobenzyl)(trifluoromethyl)sulfane(2408-08-4)

Safety Data

• Hazardous Substances Data: 2408-08-4(Hazardous Substances Data)

Upstream product

• 811-68-7 silver(I) trifluoromethanethiolate 
• 456-41-7 1-(Bromomethyl)-3-fluorobenzene 
• 1413732-47-4 (2,2'-bipyride-kN₁,kN₁')(1,1,1-trifluoromethanethiolato-kS)-copper 
• 352-70-5 m-Fluorotoluene 
• 21259-75-6 mercury bis(trifluoromethanethiolate) 
• 28490-56-4 1-fluoro-3-(iodomethyl)benzene 

Downstream Products

• 2408-22-2 3-fluorophenylmethyl trifluoromethyl sulfone 
• 2408-07-3 (3-Fluor-benzyl)-trifluormethyl-sulfoxid 

Relevant articles and documents

An efficient and practical approach to trifluoromethylthiolation of α-haloketones/α-haloarylmethanes

An efficient and practical approach to trifluoromethylthiolation of α-haloketones/α-haloarylmethanes was developed. The transformation employs only AgSCF3 and KI in situ generated active nucleophilic trifluoromethylthio species and cleanly occurs in up to quantitative yield at room temperature, thereby providing an unprecedentedly easy entry to various α-SCF3-substituted ketones/arylmethanes.

Trifluoro methylthiomethyl benzene derivatives and process for production same

The present invention lies in a process for producing a trifluoromethylthiomethylbenzene derivative represented by the following general formula (2): (wherein R is a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, an alkoxycarbonyl group,