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164798

Sigma-Aldrich

Trifluoromethanesulfonyl chloride

≥99%

Synonym(s):

Triflyl chloride

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About This Item

Linear Formula:
CF3SO2Cl
CAS Number:
421-83-0
Molecular Weight:
168.52
Beilstein/REAXYS Number:
1812106
EC Number:
207-009-0
MDL number:
MFCD00007451
UNSPSC Code:
12352101
PubChem Substance ID:
24850102
NACRES:
NA.22

vapor pressure

10.36 psi ( 20 °C)

Quality Level

100

assay

≥99%

form

liquid

refractive index

n20/D 1.334 (lit.)

bp

29-32 °C (lit.)

density

1.583 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

FC(F)(F)S(Cl)(=O)=O

InChI

1S/CClF3O2S/c2-8(6,7)1(3,4)5

InChI key

GRGCWBWNLSTIEN-UHFFFAOYSA-N

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Application

Trifluoromethanesulfonyl chloride can be used as:
  • A trifluoromethylating agent for the fluoroalkylation of heterocycles, arenes, and heteroarenes.
  • A sulfonating agent for alcohols.
  • A chlorinating agent for carbanions.

accessory

Product No.
Description
Pricing

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

supp_hazards

EUH014

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Journal of the Chemical Society. Perkin Transactions 1, 627-627 (1991)
Marleen Häring et al.
The Journal of organic chemistry, 83(15), 7928-7938 (2018-05-29)
In this work, we demonstrate that useful C-C bond-forming photoredox catalysis can be performed in air using easily prepared gel networks as reaction media to give similar results as are obtained under inert atmosphere conditions. These reactions are completely inhibited
Journal of the Chemical Society. Perkin Transactions 1, 1339-1339 (1994)

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