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6-Chloro-1H-indole-2-carbaldehyde

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6-Chloro-1H-indole-2-carbaldehyde Basic information
Product Name:6-Chloro-1H-indole-2-carbaldehyde
Synonyms:1H-Indole-2-carboxaldehyde, 6-chloro-;6-Chloro-1H-indole-2-carbaldehyde
CAS:53590-59-3
MF:C9H6ClNO
MW:179.6
EINECS:
Product Categories:
Mol File:53590-59-3.mol
6-Chloro-1H-indole-2-carbaldehyde Structure
6-Chloro-1H-indole-2-carbaldehyde Chemical Properties
Boiling point 373.4±22.0 °C(Predicted)
density 1.431±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka14.15±0.30(Predicted)
AppearanceLight yellow to brown Solid
Safety Information
HS Code 29339900
MSDS Information
6-Chloro-1H-indole-2-carbaldehyde Usage And Synthesis
Chemical PropertiesBrown solid
Synthesis
(6-CHLORO-1H-INDOL-2-YL)-METHANOL

53590-58-2

6-CHLORO-1H-INDOLE-2-CARBALDEHYDE

53590-59-3

GENERAL STEPS: A suspension of 2-hydroxymethyl-6-chloroindole (1 mmol) with activated MnO2 (10 mmol) in DMF (30 mL) was stirred at room temperature for 12 hours. After completion of the reaction, the mixture was filtered through a diatomaceous earth pad. The filtrate was concentrated under vacuum and the residue was purified by column chromatography to afford 6-chloro-1H-indole-2-carbaldehyde using EtOAc-hexane mixed solvent as eluent.

References[1] European Journal of Medicinal Chemistry, 2016, vol. 121, p. 561 - 577
[2] Patent: US2003/144282, 2003, A1
[3] Journal of Medicinal Chemistry, 2007, vol. 50, # 6, p. 1380 - 1400
[4] Patent: US2008/9485, 2008, A1. Location in patent: Page/Page column 31
[5] Journal of Medicinal Chemistry, 2014, vol. 57, # 2, p. 364 - 377
6-Chloro-1H-indole-2-carbaldehyde Preparation Products And Raw materials
Tag:6-Chloro-1H-indole-2-carbaldehyde(53590-59-3) Related Product Information
4,6-Dichloro-1H-indole-2-carbonyl chloride 6-Chloroindole-2-carboxylic acid ethyl ester 6-Chloroindole-2-carboxylic acid 4,6-Dichloro-1H-indole-2-carboxylic acid Ethyl 4,6-dichloroindole-2-carboxylate 6-Chloro-1H-indole-2-carboxylic acid methyl ester alpha-Phenyl-1-(2-phenylethyl)-4-piperidinemethanol Ethyl 4,6-dichloro-3-formyl-1H-indole-2-carboxylate 6-Chloro-4-fluoro-1H-indole-2-carboxylic acid 6-Chloro-7-methyl-1H-indole-2-carboxylic acid 6,7-Dichloro-1H-indole-2-carboxylic acid ethyl ester (Z)-2-Carboxy-4,6-dichloroindole-3-(2'-phenyl-2'-carboxy)-ene 4,6-Dichloro-3-[(1E)-3-oxo-3-(phenylamino)-1-propenyl]-1H-indole-2-carboxylic acid sodium salt Ethyl 3-(2-carboxy-vinyl)-4,6-dichloro-1H-indole-2-carboxylate 6,7-Dichloro-1H-indole-2-carboxylic acid 1H-Indole-2-carboxylic acid,6-chloro-4-fluoro-3-formyl-,ethyl ester 1-(beta-Dimethylaminoaethyl)-2-ethoxycarbonyl-3-ethoxy-6-chlor-indol-t oluol-4-sulfonat 4,6-Dichloro-3-hydroxymethyl-1H-indole-2-carboxylic acid ethyl ester