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424196

Sigma-Aldrich

2-(Trifluoroacetyl)pyrrole

99%

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About This Item

Empirical Formula (Hill Notation):
C6H4F3NO
CAS Number:
Molecular Weight:
163.10
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

solid

mp

48-50 °C (lit.)

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.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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)
Preparation of Indazoles and Quinazolines by Catalytic Dehydrogenation.
Burnett JrJ and Ainsworth C.
The Journal of Organic Chemistry, 23(9), 1382-1383 (1958)

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