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3-(Trifluoromethylthio)aniline, 96%, Thermo Scientific Chemicals
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Catalog number B23734.06
also known as B23734-06
Price (USD)/ Each
350.00
-
Quantity:
5 g
Price (USD)/ Each
350.00
3-(Trifluoromethylthio)aniline, 96%, Thermo Scientific Chemicals
Catalog numberB23734.06
Price (USD)/ Each
350.00
-
Chemical Identifiers
CAS369-68-6
Specifications
Specification Sheet
Specification SheetAssay (GC)≥95.0%
Appearance (Color)Clear colorless to red to brown
FormLiquid
Refractive Index1.5175-1.5235 @ 20°C
3-(Trifluoromethylthio)aniline is used as an intermediate in organic synthesis. It is also involved in the regioselective Friedel-Crafts alkylation in hexafluoroacetone sesquihydrate.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
3-(Trifluoromethylthio)aniline is used as an intermediate in organic synthesis. It is also involved in the regioselective Friedel-Crafts alkylation in hexafluoroacetone sesquihydrate.
Solubility
Immiscible with water.
Notes
Incompatible with strong oxidizing agents and strong bases.
3-(Trifluoromethylthio)aniline is used as an intermediate in organic synthesis. It is also involved in the regioselective Friedel-Crafts alkylation in hexafluoroacetone sesquihydrate.
Solubility
Immiscible with water.
Notes
Incompatible with strong oxidizing agents and strong bases.
RUO – Research Use Only
General References:
- Masciadri, R.; Kamer, M.; Nock, N. Regioselective Friedel-Crafts Alkylation of Anilines and Amino-Substituted Heteroarenes with Hexafluoroacetone Sesquihydrate. Eur. J. Org. Chem. 2003, 2003 (21), 4286-4291.
- Manoury, P. M.; Dumas, A. P.; Najer, H.; Branceni, D.; Prouteau, M.; Lefevre-Borg, F. M. Synthesis and analgesic activities of some (4-substituted phenyl-1-piperazinyl)alkyl 2-aminobenzoates and 2-aminonicotinates. J. Med. Chem. 1979, 22 (5), 554-559.