Basic Information |
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Product Name: | 3-(TRIFLUOROACETYL)INDOLE |
CAS: | 14618-45-2 |
English Synonyms: | 3-INDOLYL TRIFLUOROMETHYL KETONE ; 2,2,2-TRIFLUORO-1-(1H-INDOL-3-YL)ETHANONE ; 2,2,2-TRIFLUORO-1-(1H-INDOL-3-YL)-1-ETHANONE ; 2,2,2-TRIFLUORO-1-(1H-INDOL-3-YL)ETHAN-1-ONE ; 3-(TRIFLUOROACETYL)INDOLE |
MDL Number.: | MFCD00182114 |
H bond acceptor: | 2 |
H bond donor: | 1 |
Smile: | c1ccc2c(c1)c(c[nH]2)C(=O)C(F)(F)F |
InChi: | InChI=1S/C10H6F3NO/c11-10(12,13)9(15)7-5-14-8-4-2-1-3-6(7)8/h1-5,14H |
InChiKey: | InChIKey=LCMDCXWSHDFQKP-UHFFFAOYSA-N |
Property |
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Melting Point: | 211-214 DEG C(LIT) |
Comments: | APPLICATION: REACTANT FOR ENANTIOSELECTIVE SYNTHESIS OF INDOLES VIA PALLADIUM-CATALYZED KINETIC ASYMMETRICAL ALKYLATION. REACTANT FOR PREPARATION OF N-PYRIDINYL INDOLECARBOXAMIDES VIA AMIDATION OF AMINOPYRIDINE DERIVATIVES. WITH INDOLECARBOXYLIC ACID. REACTANT FOR PREPARATION OF MAST CELL TRYPTASE INHIBITORS, STARTING FROM INDOLES APPLICATION: USING AMIDATION AS THE KEY STEP. REACTANT FOR FORMATION OF MICHAEL ADDUCTS VIA BAYLIS-HILLMAN REACTION. REACTANT FOR PREPARATION OF INDOLECARBOXAMIDES VIA HALOFORM CLEAVAGE OF (TRIFLUOROACETYL)INDOLE WITH LITHIUM DIALKYLAMIDES UNSPSC: 12352100 WGK: 3 |
Safety information |
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Symbol: |
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Signal word: | Warning |
Hazard statements: | H315-H319-H335 |
Precautionary statements: | P261-P305 + P351 + P338 |
hazard symbol: | Xi |
Risk Code: | R:36/37/38 |
Safe Code: | S:26-36 |
WGK Germany: | 3 |
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