Basic information Safety Supplier Related

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

Basic information Safety Supplier Related

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

Product Name:
2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID
Synonyms:
  • 2-oxo-1,3-dihydroindole-6-carboxylic acid
  • 2-Oxoindoline-6-carboxylic acid in stock Factory
  • Nidanib Impurity 2: 2-oxy-2,3-dihydro-1H-indole-6-carboxylic acid
  • RARECHEM AL BO 0984
  • OXINDOLE-6-CARBOXYLIC ACID
  • 2,3-DIHYDRO-2-OXO-1H-INDOLE-6-CARBOXYLIC ACID
  • 2-Oxindole-6-carboxylic acid
  • 2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID
CAS:
334952-09-9
MF:
C9H7NO3
MW:
177.16
Product Categories:
  • blocks
  • Carboxes
  • IndolesOxindoles
  • pharmacetical
  • Indoline & Oxindole
Mol File:
334952-09-9.mol
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2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID Chemical Properties

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
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26
HS Code 
2933998090
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2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID Usage And Synthesis

Synthesis

14192-26-8

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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