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2,3-DIOXOINDOLINE-7-CARBOXYLIC ACID

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2,3-DIOXOINDOLINE-7-CARBOXYLIC ACID Basic information

Product Name:
2,3-DIOXOINDOLINE-7-CARBOXYLIC ACID
Synonyms:
  • 2,3-DIOXOINDOLINE-7-CARBOXYLIC ACID
  • 2,3-Dioxoindoline-7-carboxylic acid, 2,3-Dihydro-2,3-dioxo-1H-indole-7-carboxylic acid
  • 2,3-dioxo-1H-indole-7-carboxylic acid
  • 2,3-Dioxoindoline-7-Carboxylic
  • 2,3-dioxo-2,3-dihydro-1H-indole-7-carboxylic acid
  • 2,3-Dioxoindoline-7-carboxylic acid, 2,3-Dihydro-2,3-dioxo-1H-indole-7-carboxylic a
  • 1H-Indole-7-carboxylic acid, 2,3-dihydro-2,3-dioxo-
  • 2,3-dioxoindoline-7-carboxylic acid - [D85935]
CAS:
25128-35-2
MF:
C9H5NO4
MW:
191.14
EINECS:
1533716-785-6
Product Categories:
  • Carboxylic Acids
  • Carboxylic Acids
  • Fused Ring Systems
Mol File:
25128-35-2.mol
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2,3-DIOXOINDOLINE-7-CARBOXYLIC ACID Chemical Properties

Melting point:
268 °C
Density 
1.591±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
crystalline powder
pka
2.66±0.20(Predicted)
color 
Orange
CAS DataBase Reference
25128-35-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,T
Risk Statements 
36/37/38-25
Safety Statements 
26-36/37/39-37/39-45
Hazard Note 
Irritant
HS Code 
2934999090
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2,3-DIOXOINDOLINE-7-CARBOXYLIC ACID Usage And Synthesis

Synthesis

Step I. Synthesis of 2,3-dioxoindoline-7-carbonitrile

To a 100 ml three-necked flask equipped with a stirrer, a thermometer and a reflux condenser tube was added 2,3-dioxoindoline-7-carbaldehyde, hydroxylamine hydrochloride, sodium acetate, 30 mL of glacial acetic acid and 1 mL of acetic anhydride, and refluxed to react. After cooling, it was poured into ice water to precipitate a solid, filtered, washed with water and dried, and recrystallized to obtain 2,3-dioxoindoline-7-carbonitrile.

Step II, Synthesis of 2,3-dioxoindoline-7-carboxylic acid

To a 100 ml three-necked flask equipped with a stirrer, a thermometer and a reflux condenser tube was added 2,3-dioxoindoline-7-carbonitrile, NaOH, water, and refluxed to react. After cooling and filtration, the filtrate was acidified with dilute hydrochloric acid to pH<3, a solid was precipitated, filtered and dried to obtain the compound 2,3-dioxoindoline-7-carboxylic acid.

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