ChemicalBook--->CAS DataBase List--->1098340-27-2

1098340-27-2

1098340-27-2 Structure

1098340-27-2 Structure
IdentificationBack Directory
[Name]

Methyl 4-(trifluoromethyl)-1H-indole-2-carboxylate
[CAS]

1098340-27-2
[Synonyms]

Methyl 4-(trifluoromethyl)-1H-indole-2-carboxylate
4-trifluoromethyl-2-indole-3-carboxylic acid methyl ester
1H-Indole-2-carboxylic acid, 4-(trifluoromethyl)-, methyl ester
[Molecular Formula]

C11H8F3NO2
[MOL File]

1098340-27-2.mol
[Molecular Weight]

243.18
Chemical PropertiesBack Directory
[Boiling point ]

334.5±37.0 °C(Predicted)
[density ]

1.403±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

13.56±0.30(Predicted)
[Appearance]

Off-white to light yellow Solid
[InChI]

InChI=1S/C11H8F3NO2/c1-17-10(16)9-5-6-7(11(12,13)14)3-2-4-8(6)15-9/h2-5,15H,1H3
[InChIKey]

HEEQKKQXILYZNF-UHFFFAOYSA-N
[SMILES]

N1C2=C(C(C(F)(F)F)=CC=C2)C=C1C(OC)=O
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 4-(trifluoromethyl)-1H-indole-2-carboxylate(1098340-27-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Propenoic acid, 2-azido-3-[2-(trifluoromethyl)phenyl]-, methyl ester

1362860-87-4

Methyl 4-(trifluoromethyl)-1H-indole-2-carboxylate

1098340-27-2

General procedure: methyl 2-azido-3-[2-(trifluoromethyl)phenyl]prop-2-enoate (20.0 mmol) was added to preheated xylene (75 mL) in one go, and the reaction was kept at reflux for 2 hours. After completion of the reaction, the solvent was removed by rotary evaporator and the resulting crude product was purified by silica gel column chromatography with the eluent being a mixed petroleum ether/ethyl acetate solvent. The synthesis of compound 4-(trifluoromethyl)-1H-indole-2-carboxylic acid methyl ester was carried out with reference to the methods reported in literature [9b], [13] and [14].

[References]

[1] European Journal of Medicinal Chemistry, 2012, vol. 49, p. 379 - 396
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