ChemicalBook--->CAS DataBase List--->334952-09-9

334952-09-9

334952-09-9 Structure

334952-09-9 Structure
IdentificationBack Directory
[Name]

2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID
[CAS]

334952-09-9
[Synonyms]

6-CARBOXYOXINDOLE
RARECHEM AL BO 0984
6-Carboxyl-2-oxindole
6-OXINDOLECARBOXYLIC ACID
OXINDOLE-6-CARBOXYLIC ACID
2-Oxindole-6-carboxylic acid
2-Oxyindole-6-carboxylic acid
2-Oxo-indoline-6-carboxylic acid
2-oxo-1,3-dihydroindole-6-carboxylic acid
2,3-DIHYDRO-2-OXO-1H-INDOLE-6-CARBOXYLIC ACID
2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID
1H-Indole-6-carboxylic acid, 2,3-dihydro-2-oxo-
2,3-Dihydro-2-oxo-1H-indole-6-carboxylic acid97%
2-Oxoindoline-6-carboxylic acid in stock Factory
Nidanib Impurity 2: 2-oxy-2,3-dihydro-1H-indole-6-carboxylic acid
[Molecular Formula]

C9H7NO3
[MDL Number]

MFCD01415801
[MOL File]

334952-09-9.mol
[Molecular Weight]

177.16
Chemical PropertiesBack Directory
[Boiling point ]

438.1±45.0 °C(Predicted)
[density ]

1.433±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

3.94±0.20(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H335-H315-H319
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[Hazard Codes ]

Xi
[Risk Statements ]

36
[Safety Statements ]

26
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID(334952-09-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl 2-oxoindole-6-carboxylate

14192-26-8

2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID

334952-09-9

General procedure for the synthesis of 2-oxoindoline-6-carboxylic acid from methyl 2-oxoindoline-6-carboxylate: Sodium hydroxide solution (1N, 20 mL) was added to a solution of 2-oxoindoline-6-carboxylic acid methyl ester (2 g, 10.46 mmol, 1.00 equiv) in methanol (20 mL). The reaction mixture was stirred at 80 °C for 2 hours. After completion of the reaction, the mixture was cooled to 30 °C, diluted with 50 mL of water and extracted with dichloromethane (2 x 30 mL). The aqueous phases were combined and the pH was adjusted with aqueous hydrochloric acid (6N) to 2. The precipitated solid was collected by filtration and dried to give the title compound 1.28 g (69% yield) as a brown solid.1H NMR (400 MHz, CDCl3) δ: 12.86 (s, 1H), 10.50 (s, 1H), 7.55 (m, 1H), 7.32-7.30 (m. 2H), 3.56 (s, 2H).

[References]

[1] Patent: US2015/284327, 2015, A1. Location in patent: Paragraph 0215; 0216
[2] Patent: WO2006/64044, 2006, A1. Location in patent: Page/Page column 21-22
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