752924
2,2,2-Trifluoroethyl trifluoromethanesulfonate
95%
Synonym(s):
Trifluoromethanesulfonic acid 2,2,2-trifluoroethyl ester
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About This Item
Empirical Formula (Hill Notation):
C3H2F6O3S
CAS Number:
Molecular Weight:
232.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352101
MDL number:
Assay:
95%
Form:
liquid
Quality Level
assay
95%
form
liquid
refractive index
n20/D 1.306
density
1.611 g/mL at 25 °C
functional group
fluoro, triflate
storage temp.
2-8°C
SMILES string
FC(F)(F)COS(=O)(=O)C(F)(F)F
InChI
1S/C3H2F6O3S/c4-2(5,6)1-12-13(10,11)3(7,8)9/h1H2
InChI key
RTMMSCJWQYWMNK-UHFFFAOYSA-N
Application
Reagent used in thenantioselective preparation of cyclic N-aryl hydroxamic acids via phase-transfer catalyzed alkylation of nitrobenzyl bromides to give nirophenylalanines
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Skin Corr. 1B
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Related Content
Baran Reagents - FAQ
Laura A McAllister et al.
The Journal of organic chemistry, 76(9), 3484-3497 (2011-04-02)
We describe a generalized approach to stereocontrolled synthesis of substituted cyclic hydroxamic acids (3-amino-1-hydroxy-3,4-dihydroquinolinones) by selective reduction of substituted 2-nitrophenylalanine substrates. Compounds in this series have antibacterial properties and have also recently been reported as KAT II inhibitors. The key
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 752924-5G | 04061833339831 |