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  8. N-Phenylbis(trifluoromethanesulfonimide), 99%, Thermo Scientific Chemicals

N-Phenylbis(trifluoromethanesulfonimide), 99%, Thermo Scientific Chemicals

Catalog Number AAL1253114
Click to view available options
Quantity:
5 g
25 g
37595-74-7
C8H5F6NO4S2
357.241
MFCD00000404
DIOHEXPTUTVCNX-UHFFFAOYSA-N
n,n-bis trifluoromethylsulfonyl aniline, phenyl triflimide, n-phenyl-bis trifluoromethanesulfonimide, n-phenyltrifluoromethanesulfonimide, n,n-bis-trifluoromethanesulfonyl aniline, 1,1,1-trifluoro-n-phenyl-n-trifluoromethylsulfonyl methanesulfonamide, n-phenylbis trifluoromethanesulfonimide, n-phenylbis trifluoromethanesulphonimide, 1,1,1-trifluoro-n-phenyl-n-trifluoromethyl sulfonyl methanesulfonamide, n,n-bis trifluoromethanesulfonyl aniline
142176
1,1,1-trifluoro-N-phenyl-N-(trifluoromethylsulfonyl)methanesulfonamide
C1=CC=C(C=C1)N(S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F
37595-74-7
C8H5F6NO4S2
357.241
MFCD00000404
DIOHEXPTUTVCNX-UHFFFAOYSA-N
n,n-bis trifluoromethylsulfonyl aniline, phenyl triflimide, n-phenyl-bis trifluoromethanesulfonimide, n-phenyltrifluoromethanesulfonimide, n,n-bis-trifluoromethanesulfonyl aniline, 1,1,1-trifluoro-n-phenyl-n-trifluoromethylsulfonyl methanesulfonamide, n-phenylbis trifluoromethanesulfonimide, n-phenylbis trifluoromethanesulphonimide, 1,1,1-trifluoro-n-phenyl-n-trifluoromethyl sulfonyl methanesulfonamide, n,n-bis trifluoromethanesulfonyl aniline
142176
1,1,1-trifluoro-N-phenyl-N-(trifluoromethylsulfonyl)methanesulfonamide
C1=CC=C(C=C1)N(S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F

Description

N-Phenylbis(trifluoromethanesulfonimide) acts as a mild triflating reagent as well as a transparent strong electron-withdrawing p-type dopant in carbon nanotubes. It is also employed as a reactant for the preparation of amphoteric alfa-boryl aldehydes. It plays an important role in the enantioselective synthesis of the core ring skeleton of leucosceptroids A-D and in steroselective sulfoxidation. Further, it is used in the enantioselective synthesis of beta-amino acids through the Mannich reaction. In addition to this, it is used in the preparation of sphingosine 1-phosphate-1 receptor agonists.

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
N-Phenylbis(trifluoromethanesulfonimide) acts as a mild triflating reagent as well as a transparent strong electron-withdrawing p-type dopant in carbon nanotubes. It is also employed as a reactant for the preparation of amphoteric alfa-boryl aldehydes. It plays an important role in the enantioselective synthesis of the core ring skeleton of leucosceptroids A-D and in steroselective sulfoxidation. Further, it is used in the enantioselective synthesis of beta-amino acids through the Mannich reaction. In addition to this, it is used in the preparation of sphingosine 1-phosphate-1 receptor agonists.

Solubility
Soluble in methanol. Slightly soluble in chloroform and ethyl acetate.

Notes
Hygroscopic. Store in a cool place. Moisture sensitive. Incompatible with strong oxidizing agents.
TRUSTED_SUSTAINABILITY
Melting Point 100°C to 102°C
Quantity 25 g
Beilstein 1269141
Sensitivity Moisture sensitive
Solubility Information Soluble in methanol. Slightly soluble in chloroform and ethyl acetate.
Formula Weight 357.25
Percent Purity 99%
Chemical Name or Material N-Phenylbis(trifluoromethanesulfonimide)

Safety and Handling

Hazard Category H315-H319-H335
Hazard Statement GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Precautionary Statement P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
TSCA No
Recommended Storage Ambient temperatures
SDS

RUO – Research Use Only

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