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N-Phenylbis(trifluoromethanesulfonimide), 99%

CAS: 37595-74-7 | C8H5F6NO4S2 | 357.241 g/mol

$129.03 - $483.21

Chemical Identifiers

CAS 37595-74-7
Molecular Formula C8H5F6NO4S2
Molecular Weight (g/mol) 357.241
MDL Number MFCD00000404
InChI Key DIOHEXPTUTVCNX-UHFFFAOYSA-N
Synonym 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
PubChem CID 142176
IUPAC Name 1,1,1-trifluoro-N-phenyl-N-(trifluoromethylsulfonyl)methanesulfonamide
SMILES C1=CC=C(C=C1)N(S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F
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Products 2
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAL1253106
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Thermo Scientific Chemicals
L1253106
5 g
Each for $129.03
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AAL1253114
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Thermo Scientific Chemicals
L1253114
25 g
Each for $483.21
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Description

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.
Specifications

Chemical Identifiers

37595-74-7
357.241
DIOHEXPTUTVCNX-UHFFFAOYSA-N
142176
C1=CC=C(C=C1)N(S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F
C8H5F6NO4S2
MFCD00000404
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
1,1,1-trifluoro-N-phenyl-N-(trifluoromethylsulfonyl)methanesulfonamide

Specifications

37595-74-7
C8H5F6NO4S2
5 g
Moisture sensitive
Soluble in methanol. Slightly soluble in chloroform and ethyl acetate.
C1=CC=C(C=C1)N(S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F
357.241
357.25
N-Phenylbis(trifluoromethanesulfonimide)
100°C to 102°C
MFCD00000404
1269141
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
DIOHEXPTUTVCNX-UHFFFAOYSA-N
1,1,1-trifluoro-N-phenyl-N-(trifluoromethylsulfonyl)methanesulfonamide
142176
99%
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Safety and Handling

Safety and Handling

GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c

H315-H319-H335

TSCA : No

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only