424196
2-(Trifluoroacetyl)pyrrole
99%
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About This Item
Empirical Formula (Hill Notation):
C6H4F3NO
CAS Number:
Molecular Weight:
163.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
solid
Quality Level
assay
99%
form
solid
mp
48-50 °C (lit.)
functional group
fluoro, ketone
SMILES string
FC(F)(F)C(=O)c1ccc[nH]1
InChI
1S/C6H4F3NO/c7-6(8,9)5(11)4-2-1-3-10-4/h1-3,10H
InChI key
UMVVPYXSJKIFST-UHFFFAOYSA-N
General description
2-(Trifluoroacetyl)pyrrole, an α,α,α-trifluoromethyl ketone is a 2-substituted pyrrole derivative. It has been synthesized by reacting pyrrole with trifluoroacetic anhydride in benzene at 0°C. Its enantioselective hydrogenation to form corresponding alcohol using 5wt.% Pt/Al2O3 catalyst chirally modified by new synthetic chiral amines has been investigated.
signalword
Warning
hcodes
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
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Find documentation for the products that you have recently purchased in the Document Library.
Preparation of Indazoles and Quinazolines by Catalytic Dehydrogenation.
Burnett JrJ and Ainsworth C.
The Journal of Organic Chemistry, 23(9), 1382-1383 (1958)
Chemo and enantioselective hydrogenation of fluorinated ketones on platinum modified with (R)-1-(1-naphthyl) ethylamine derivatives.
Diezi S, et al.
J. Mol. Catal. A: Chem., 239(1), 49-56 (2005)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 424196-5G | 04061833372555 |