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511188

Sigma-Aldrich

Methyl indole-5-carboxylate

99%

Sinónimos:

Indole-5-carboxylic acid, methyl ester

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About This Item

Fórmula empírica (notación de Hill):
C10H9NO2
Número de CAS:
1011-65-0
Peso molecular:
175.18
MDL number:
MFCD00153023
UNSPSC Code:
12352100
PubChem Substance ID:
24873426
NACRES:
NA.22

assay

99%

mp

126-128 °C (lit.)

SMILES string

COC(=O)c1ccc2[nH]ccc2c1

InChI

1S/C10H9NO2/c1-13-10(12)8-2-3-9-7(6-8)4-5-11-9/h2-6,11H,1H3

InChI key

DRYBMFJLYYEOBZ-UHFFFAOYSA-N

General description

Methyl indole-5-carboxylate (Methyl 1H-indole-5-carboxylate), a substituted 1H-indole, can be prepared by the esterification of indole-5-carboxylic acid. Its efficacy as a substrate for indigoid generation has been assessed.

Application

Methyl indole-5-carboxylate may be used as a reactant in the following processes:
  • biosynthesis of inhibitors of protein kinases
  • metal-free Friedel-Crafts alkylation
  • preparation of diphenylsulfonium ylides from Martin′s sulfurane
  • cross dehydrogenative coupling reactions
  • synthesis of indirubin derivatives
  • preparation of aminoindolylacetates
Methyl indole-5-carboxylate may be used in the preparation of:
  • methyl indoline-5-carboxylate
  • 1H-indole-5-carbohydrazide
  • dimethyl 1H-indole-3,5-dicarboxylate

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Fei Yang et al.
Organic letters, 12(22), 5214-5217 (2010-10-23)
A novel cross dehydrogenative coupling (CDC) reaction of N,N-dimethylanilines with methyl ketones by cooperative copper and aminocatalysis has been developed, which leads to the formation of β-arylamino ketones in 42-73% yields. Moreover, the copper-catalyzed alkylation of free (NH) indoles with
Wang, T. C.; et al.
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 21, 1407-1407 (2010)
Liu, Z.; et al.
Letters in Organic Chemistry, 7, 666-666 (2010)
Wen-Jie Lu et al.
European journal of medicinal chemistry, 64, 498-511 (2013-05-21)
This report describes the synthesis, and in vitro and in vivo antimalarial evaluations of certain ester-modified neocryptolepine (5-methyl-5H-indolo[2,3-b]quinoline) derivatives. The modifications were carried out by introducing ester groups at the C2 and/or C9 position on the neocryptolepine core and the
A facial synthesis and antimicrobial activity of some pyrazole derivatives carrying indole.
Sarma KN, et al.
Journal of Chemistry, 7(3), 745-750 (2010)
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