Substance
ID:331423
Names and Identifiers
IUPAC Traditional name
8-(trifluoromethyl)-8-thiatricyclo[7.4.0.02,7]trideca-1(13),2,4,6,9,11-hexaen-8-ium tetrafluoroborate
Synonyms
5-(Trifluoromethyl)dibenzothiophenium tetrafluoroborate5-(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
Properties
Safety Information
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
MSDS Link
German water hazard class
3
Product Information
Empirical Formula (Hill Notation)
C13H8BF7S
Purity
97%
Physical Property
Melting Point
162-164 °C(lit.)
Molecule Details
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
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
Molecular Spectra
No Data Available
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References
No Data Available
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