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5-(Trifluoromethyl)dibenzothiophenium tetrafluoroborate_Molecular_structure_CAS_131880-16-5)
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5-(Trifluoromethyl)dibenzothiophenium tetrafluoroborate

Catalog No. 483869 Name Sigma Aldrich
CAS Number 131880-16-5 Website http://www.sigmaaldrich.com
M. F. C13H8BF7S Telephone 1-800-521-8956
M. W. 340.0674424 Fax
Purity 97% Email
Storage Chembase ID: 97458

SYNONYMS

Title
5-(三氟甲基)二苯并噻吩鎓四氟硼酸盐
IUPAC name
8-(trifluoromethyl)-8-thiatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaen-8-ium; tetrafluoroboranuide
IUPAC Traditional name
8-(trifluoromethyl)-8-thiatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaen-8-ium tetrafluoroborate

DATABASE IDS

CAS Number 131880-16-5
MDL Number MFCD01073545
PubChem SID 24871922

PROPERTIES

Empirical Formula (Hill Notation) C13H8BF7S
Purity 97%
Melting Point 162-164 °C(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (English)
Packaging
1 g in glass bottle
Application

• Pd(II)-catalyzed trifluoromethylation1
• Copper-catalyzed trifluoromethylation of aryl boronic acids using a Collidine as a trifluoromethylating reagent2
• Pd-catalyzed electrophilic ortho-trifluoromethylation of arenes3 Used in the stereoselective preparation of
• Trifluoromethyl-substituted alkenes via copper-catalyzed trifluoromethylation of terminal alkenes4
• Trifluoromethyl-bearing quaternary carbon centers by Pd-catalyzed intramolecular decarboxylative allylation of α-trifluoromethyl β-keto esters5
Description (简体中文)
包装
1 g in glass bottle
Application

• Pd(II)-catalyzed trifluoromethylation1
• Copper-catalyzed trifluoromethylation of aryl boronic acids using a Collidine as a trifluoromethylating reagent2
• Pd-catalyzed electrophilic ortho-trifluoromethylation of arenes3 Used in the stereoselective preparation of
• Trifluoromethyl-substituted alkenes via copper-catalyzed trifluoromethylation of terminal alkenes4
• Trifluoromethyl-bearing quaternary carbon centers by Pd-catalyzed intramolecular decarboxylative allylation of α-trifluoromethyl β-keto esters5

REFERENCES