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Phenyl trifluoromethyl sulfide_Molecular_structure_CAS_456-56-4)
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Phenyl trifluoromethyl sulfide

Catalog No. 511196 Name Sigma Aldrich
CAS Number 456-56-4 Website http://www.sigmaaldrich.com
M. F. C7H5F3S Telephone 1-800-521-8956
M. W. 178.1748096 Fax
Purity 99% Email
Storage Chembase ID: 8490

SYNONYMS

Title
三氟甲基苯硫醚
IUPAC name
[(trifluoromethyl)sulfanyl]benzene
IUPAC Traditional name
trifluoromethylthiobenzene
Synonyms
[(Trifluoromethyl)thio]benzene
Trifluoromethyl phenyl thioether

DATABASE IDS

EC Number 207-270-0
PubChem SID 24873427
MDL Number MFCD00040839
CAS Number 456-56-4

PROPERTIES

Linear Formula C6H5SCF3
Purity 99%
Boiling Point 142 °C(lit.)
Density 1.249 g/mL at 25 °C(lit.)
Flash Point 37 °C
Flash Point 98.6 °F
Refractive Index n20/D 1.466(lit.)
GHS Pictograms GHS02
GHS Signal Word Warning
GHS Hazard statements H226
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
RID/ADR UN 1993 3/PG 3
Risk Statements 10
Safety Statements 16-36
Hazard Class 3
UN Number 1993
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
Packaging
5 g in glass bottle
Application
Used in the preparation of
• Sulfoxides, dithiane dioxide, and dithiolane dioxide via iron-catalyzed oxidation of sulfides, dithiane, or dithiolane with hydrogen peroxide1
• Used in the preparation of benzophenone hydrazone derivatives as insecticides2
• Reductive silylation and the preparation of trifluoro- and difluoromethylsilanes by reductive coupling of fluoromethyl sulfones, sulfoxides and sulfides with chlorosilanes3
Description (简体中文)
包装
5 g in glass bottle
Application
Used in the preparation of
• Sulfoxides, dithiane dioxide, and dithiolane dioxide via iron-catalyzed oxidation of sulfides, dithiane, or dithiolane with hydrogen peroxide1
• Used in the preparation of benzophenone hydrazone derivatives as insecticides2
• Reductive silylation and the preparation of trifluoro- and difluoromethylsilanes by reductive coupling of fluoromethyl sulfones, sulfoxides and sulfides with chlorosilanes3

REFERENCES