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N-Phenyl-bis(trifluoromethanesulfonimide)

ALDRICH/295973 - 99%

Synonym: 1,1,1-Trifluoro-N-phenyl-N-[(trifluoromethyl)sulfonyl]methanesulfonamide; N,N-Bis(trifluoromethylsulfonyl)aniline; N-Phenyl-trifluoromethanesulfonimide; NSC 240874; Phenyl triflimide

CAS Number: 37595-74-7
Empirical Formula (Hill Notation): C8H5F6NO4S2
Molecular Weight: 357.25
MDL Number: MFCD00000404
Linear Formula: C6H5N(SO2CF3)2
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-295973-5G 5 g
 $90.10
1/EA		 Add To Favorites
45-295973-25G 25 g
 $220.00
1/EA		 Add To Favorites
This picture is provided solely for illustration purposes, it may have been created or edited with AI. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 295973-5G
ATR-IR Spectra for 1,1,1-Trifluoro-N-phenyl-N-[(trifluoromethyl)sulfonyl]methanesulfonamide.
FT-NMR Spectra for 1,1,1-Trifluoro-N-phenyl-N-[(trifluoromethyl)sulfonyl]methanesulfonamide.
FT-IR Spectra for 1,1,1-Trifluoro-N-phenyl-N-[(trifluoromethyl)sulfonyl]methanesulfonamide.

 

assay 99%
form solid
functional group fluoro
InChI 1S/C8H5F6NO4S2/c9-7(10,11)20(16,17)15(6-4-2-1-3-5-6)21(18,19)8(12,13)14/h1-5H
InChI key DIOHEXPTUTVCNX-UHFFFAOYSA-N
mp 100-102 °C (lit.)
Quality Level 200 
SMILES string FC(F)(F)S(=O)(=O)N(c1ccccc1)S(=O)(=O)C(F)(F)F
Application: Acts as a transparent strong electron-withdrawing p-type dopant in carbon nanotubes

Reactant for:
Synthesis of amphoteric alpha-boryl aldehydes
Enantioselective synthesis of core ring skeleton of leucosceptroids A-D
Stereoselective synthesis of monoamine reuptake inhibitor NS9544 acetate
Stereoselective sulfoxidation
Application: Mild triflating reagent.
Application: Used recently to convert a ketone to an enol triflate with KHMDS (324671) and thence an olefin with Pd(PPh3)4 (216666) and Bu3SnH (234788).
Packaging: 5, 25 g in glass bottle
Purity 99%
mp 100-102 °C (lit.)
UNSPSC 12352002

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