Home > Compound List > Product Information
3-(Trifluoroacetyl)indole_Molecular_structure_CAS_14618-45-2)
Click picture or here to close

3-(Trifluoroacetyl)indole

Catalog No. 422223 Name Sigma Aldrich
CAS Number 14618-45-2 Website http://www.sigmaaldrich.com
M. F. C10H6F3NO Telephone 1-800-521-8956
M. W. 213.1559496 Fax
Purity 99% Email
Storage Chembase ID: 41692

SYNONYMS

Title
3-(三氟乙酰基)吲哚
IUPAC name
2,2,2-trifluoro-1-(1H-indol-3-yl)ethan-1-one
IUPAC Traditional name
INDOLE3trifluoroacetyl
Synonyms
3-Indolyl trifluoromethyl ketone

DATABASE IDS

MDL Number MFCD00182114
PubChem SID 24866420
CAS Number 14618-45-2

PROPERTIES

Empirical Formula (Hill Notation) C10H6F3NO
Purity 99%
Melting Point 211-214 °C(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Packaging
1, 5 g in glass bottle
Application

• Reactant for enantioselective synthesis of indoles via palladium-catalyzed kinetic asymmetrical alkylation1
• Reactant for preparation of N-pyridinyl indolecarboxamides via amidation of aminopyridine derivatives. with indolecarboxylic acid2
• Reactant for preparation of mast cell tryptase inhibitors, starting from indoles; using amidation as the key step3
• Reactant for formation of Michael adducts via Baylis-Hillman reaction4
• Reactant for preparation of indolecarboxamides via haloform cleavage of (trifluoroacetyl)indole with lithium dialkylamides5
Description (简体中文)
包装
1, 5 g in glass bottle
Application

• Reactant for enantioselective synthesis of indoles via palladium-catalyzed kinetic asymmetrical alkylation1
• Reactant for preparation of N-pyridinyl indolecarboxamides via amidation of aminopyridine derivatives. with indolecarboxylic acid2
• Reactant for preparation of mast cell tryptase inhibitors, starting from indoles; using amidation as the key step3
• Reactant for formation of Michael adducts via Baylis-Hillman reaction4
• Reactant for preparation of indolecarboxamides via haloform cleavage of (trifluoroacetyl)indole with lithium dialkylamides5

REFERENCES