Trifluoromethylthiobenzene

Trifluoromethylthiobenzene Basic information
Product Name:Trifluoromethylthiobenzene
Synonyms:[(Trifluoromethyl)sulfanyl]benzene;Benzene, [(trifluoromethyl)thio]-;ALPHA,ALPHA,ALPHA-TRIFLUOROTHIOANISOLE;PHENYL TRIFLUOROMETHYL SULFIDE;PHENYL TRIFLUOROMETHYL SULPHIDE;(TRIFLUOROMETHYLTHIO)BENZENE;TRIFLUOROMETHYL PHENYL SULFIDE;Trifluoromethyl phenyl sulphide~(Trifluoromethylthio)benzene~alpha,alpha,alpha-Trifluorothioanisole
CAS:456-56-4
MF:C7H5F3S
MW:178.17
EINECS:207-270-0
Product Categories:Organic Building Blocks;Sulfides/Disulfides;Sulfur Compounds
Mol File:456-56-4.mol
Trifluoromethylthiobenzene Structure
Trifluoromethylthiobenzene Chemical Properties
Boiling point 142 °C (lit.)
density 1.249 g/mL at 25 °C (lit.)
refractive index n20/D 1.466(lit.)
Fp 100 °F
form clear liquid
color Colorless to Almost colorless
Sensitive Stench
BRN 2043134
CAS DataBase Reference456-56-4(CAS DataBase Reference)
NIST Chemistry ReferencePhenyl trifluoromethyl sulfide(456-56-4)
Safety Information
Hazard Codes T
Risk Statements 10-36/37/38
Safety Statements 16-36-36/37/39-23
RIDADR UN 1993 3/PG 3
WGK Germany 3
Hazard Note Toxic/Stench
HazardClass 3
PackingGroup III
HS Code 29309090
MSDS Information
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Phenyl trifluoromethyl sulfide English
SigmaAldrich English
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Trifluoromethylthiobenzene Usage And Synthesis
UsesPhenyl trifluoromethyl sulfide may be used in the preparation of:
  • sulfoxides, dithiane dioxide, and dithiolane dioxide via iron-catalyzed oxidation of sulfides, dithiane, or dithiolane with hydrogen peroxide
  • benzophenone hydrazone derivatives
  • trifluoro- and difluoromethylsilanes by reductive coupling of fluoromethyl sulfones, sulfoxides and sulfides with chlorosilanes
Synthesis Reference(s)The Journal of Organic Chemistry, 50, p. 4047, 1985 DOI: 10.1021/jo00221a017
Synthesis, p. 721, 1975 DOI: 10.1055/s-1975-23905
General DescriptionPhenyl trifluoromethyl sulfide (PTFMS) is an aryl trifluoromethyl sulfide. PTFMS with (triethylgermyl)sodium forms a reagent system that has been employed for the trifluoromethylation of certain imines. The reaction between OH radical and PTFMS has been analyzed using pulse radiolysis technique and quantum chemical calculations.
Trifluoromethylthiobenzene Preparation Products And Raw materials
Trityl candesartan cilexetil Hydrogen Sulfide 4-(Trifluoromethylthio)benzonitrile Diphenyl sulfide 3-(Trifluoromethyl)benzaldehyde PHENYL RESIN 4-(Trifluoromethylthio)chlorobenzene 2-(Trifluoromethyl)benzoic acid CARBONYL SULFIDE 4-(TRIFLUOROMETHYLTHIO)BENZOIC ACID Trifluoromethyl PHENYL VALERATE 4-(TRIFLUOROMETHYLTHIO)TOLUENE 2-(Trifluoromethyl)benzaldehyde Trifluoromethylthiobenzene 4-(Trifluoromethylthio)nitrobenzene 2-(3-(1-ETHYL-3-(3-SULFOPROPYL)-5-(TRIFLUOROMETHYLSULFONYL)-1,3-DIHYDRO-2H-BENZIMIDAZOL-2-YLIDENE)-1-PROPENYL)-1-ETHYL-3-(3-SULFOPROPYL)-5-(TRIFLUOROMETHYLSULFONYL)-1H-BENZIMIDAZOLIUM NA+ 4'-(Trifluoromethyl)acetophenone

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