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197506-83-5

197506-83-5 Structure

197506-83-5 Structure
IdentificationBack Directory
[Name]

3-FORMYL-1H-INDOLE-5-CARBOXYLIC ACID METHYL ESTER
[CAS]

197506-83-5
[Synonyms]

RARECHEM AH BS 0103
Methyl 3-forMylindole-5-c...
METHYL 3-FORMYLINDOLE-5-CARBOXYLATE
METHYL 3-FORMYL-1H-INDOLE-5-CARBOXYLATE
3-FORMYLINDOLE-5-CARBOXYLIC ACID METHYL ESTER
INDOLE-3-ALDEHYDE-5-CARBOXYLIC ACID METHYL ESTER
3-FORMYL-1H-INDOLE-5-CARBOXYLIC ACID METHYL ESTER
1H-Indole-5-carboxylic acid, 3-formyl-, methyl ester
INDOLE-3-CARBOXALDEHYDE-5-CARBOXYLIC ACID METHYL ESTER
[Molecular Formula]

C11H9NO3
[MDL Number]

MFCD00211075
[MOL File]

197506-83-5.mol
[Molecular Weight]

203.19
Chemical PropertiesBack Directory
[Boiling point ]

404.4±25.0 °C(Predicted)
[density ]

1.341±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

14.59±0.30(Predicted)
[Appearance]

Off-white to light yellow Solid
[CAS DataBase Reference]

197506-83-5
Questions And AnswerBack Directory
[Uses]

3-Aldehydeindole-5-carboxylic acid methyl ester is a carboxylic acid ester derivative that can be used as a pharmaceutical and chemical intermediate.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Spectrum DetailBack Directory
[Spectrum Detail]

3-FORMYL-1H-INDOLE-5-CARBOXYLIC ACID METHYL ESTER(197506-83-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl indole-5-carboxylate

1011-65-0

N,N-Dimethylformamide

68-12-2

3-FORMYL-1H-INDOLE-5-CARBOXYLIC ACID METHYL ESTER

197506-83-5

Methyl 1H-indole-5-carboxylate (11 g, 62.3 mmol) was dissolved in 100 mL of N,N-dimethylformamide (DMF) at 0 °C and phosphorus oxychloride (POCl3, 7.9 mL, 84.8 mmol) was added slowly. The reaction mixture was stirred at room temperature for 2 hours. Upon completion of the reaction, the reaction was quenched by the addition of 350 mL of water and the mixture was heated to reflux for 15 minutes to form a brown suspension. After cooling to room temperature, a large amount of precipitate was observed to be generated. Subsequently, an additional 300 mL of water was added and stirring was continued for 10 minutes. The solid product was collected by filtration, washed sequentially with water and hexane, and finally dried under vacuum at 60 °C overnight to afford methyl 3-formylindole-5-carboxylate (12.7 g, 99.5% yield) as a pale pink solid.

[References]

[1] Patent: US2006/276496, 2006, A1. Location in patent: Page/Page column 62; 63
[2] Patent: WO2017/136395, 2017, A1. Location in patent: Page/Page column 263
[3] Chemistry - A European Journal, 2016, vol. 22, # 2, p. 716 - 723
[4] Patent: US2012/309757, 2012, A1. Location in patent: Page/Page column 170
[5] Journal of Antibiotics, 2017, vol. 70, # 7, p. 832 - 844
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