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403636

N-(2-Pyridyl)bis(trifluoromethanesulfonimide)

96%

Synonym(s):

2-[N,N-Bis(trifluoromethylsulfonyl)amino]pyridine, N,N-Bis(trifluoromethylsulfonyl)-2-pyridylamine

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5 G

$276.00

$276.00


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About This Item

Empirical Formula (Hill Notation):
C7H4F6N2O4S2
CAS Number:
Molecular Weight:
358.24
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5832565

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Product Name

N-(2-Pyridyl)bis(trifluoromethanesulfonimide), 96%

InChI

1S/C7H4F6N2O4S2/c8-6(9,10)20(16,17)15(5-3-1-2-4-14-5)21(18,19)7(11,12)13/h1-4H

SMILES string

FC(F)(F)S(=O)(=O)N(c1ccccn1)S(=O)(=O)C(F)(F)F

InChI key

DXLQEJHUQKKSRB-UHFFFAOYSA-N

assay

96%

form

solid

bp

80-90 °C/0.25 mmHg (lit.)

mp

40-42 °C (lit.)

functional group

fluoro

storage temp.

2-8°C

Quality Level

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1 of 4

This Item
40364429597378175
assay

96%

assay

96%

assay

99%

assay

≥98.0% (HPLC)

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

200

form

solid

form

solid

form

solid

form

crystals

mp

40-42 °C (lit.)

mp

45-47 °C (lit.)

mp

100-102 °C (lit.)

mp

100-102 °C (lit.)

bp

80-90 °C/0.25 mmHg (lit.)

bp

-

bp

-

bp

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

-

storage temp.

-

Application

N-(2-Pyridyl)bis(trifluoromethanesulfonimide) may be used in the synthesis of aryl triflates and vinyl triflates.[1]

General description

N-(2-Pyridyl)bis(trifluoromethanesulfonimide) (2-[N,N-Bis(trifluoromethylsulfonyl)amino]pyridine, N,N-Bis(trifluoromethylsulfonyl)-2-pyridylamine)) is a useful triflating reagent. It has been synthesized by reacting 2-aminopyridine and triflic anhydride.[1]

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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N-(2-Pyridyl) bis (trifluoromethanesulfonimide).
Cossy J and Allais F.
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2007)

Articles

Chiral diene ligands enable asymmetric transformations, constructing enantioenriched compounds from achiral substrates efficiently.

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