3-(三氟乙酰基)吲哚

pro_cas
14618-45-2
pro_cdbregno
CCD00088295
pro_formula
C10 H6 F3 N O
pro_molWeight
213.157

basic_info

Product_Name: 3-(三氟乙酰基)吲哚
CAS: 14618-45-2
中文同义词: 3-三氟乙酰基吲哚 ; 2,2,2-三氟-1-(1H-吲哚-3-基)-1-乙酮 ; 3-(三氟乙酰基)吲哚
EnglishSynonyms: 2,2,2-TRIFLUORO-1-(1H-INDOL-3-YL)-1-ETHANONE ; 3-(TRIFLUOROACETYL)INDOLE ; 2,2,2-TRIFLUORO-1-(1H-INDOL-3-YL)ETHANONE ; 2,2,2-TRIFLUORO-1-(1H-INDOL-3-YL)ETHAN-1-ONE ; 3-INDOLYL TRIFLUOROMETHYL KETONE
pro_mdlNumber: MFCD00182114
pro_acceptors: 2
pro_donors: 1
pro_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

MeltingPoint: 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

secure_info

secure_symbol: GHS07 GHS07
secure_signal_word: Warning
secure_risk_stmt: H315-H319-H335
secure_cautionary_stmt: P261-P305 + P351 + P338
secure_damage_code: Xi
secure_risk_disclosure_stmt: R:36/37/38
secure_security_stmt: S:26-36
secure_wgk_germany: 3

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