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5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione

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Products Intro: Product Name:2,3-Pyridinedicarboximide
CAS:4664-00-0
Purity:98%(Min,HPLC) Package:1G;1KG;100KG
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Products Intro: Product Name:2,3-Pyridinedicarboximide
CAS:4664-00-0
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Products Intro: Product Name:5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione
CAS:4664-00-0
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-20557
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Products Intro: Product Name:3,4-pyridinedicarboximide
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Products Intro: Product Name:QUINOLINIMIDE
CAS:4664-00-0
Purity:99% Package:1KG;1USD

5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione manufacturers

  • QUINOLINIMIDE
  • QUINOLINIMIDE  pictures
  • $1.10 / 1g
  • 2025-11-18
  • CAS:4664-00-0
  • Min. Order: 1g
  • Purity: 99.00%
  • Supply Ability: 100 Tons Min
  • QUINOLINIMIDE
  • QUINOLINIMIDE pictures
  • $1.00 / 1KG
  • 2020-01-05
  • CAS:4664-00-0
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 200kg
5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione Basic information
Product Name:5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione
Synonyms:pyridine-2,3-dicarboximide;QUINOLINICACIDAMIDE;2,3-Pyridinedicarbimide;6H-Pyrrolo[3,4-b]pyridine-5,7-dione;Pyridine-2,3-dicarbimide;3,4-Pyridinedicarboximide;NSC 405554;2,3-PYRIDINEDICARBOXAMIDE
CAS:4664-00-0
MF:C7H4N2O2
MW:148.12
EINECS:225-107-1
Product Categories:Heterocycle-Pyridine series;Pyridine;Miscellaneous Reagents;Aromatics;Heterocycles
Mol File:4664-00-0.mol
5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione Structure
5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione Chemical Properties
Melting point 233-234°C
Boiling point 268.69°C (rough estimate)
density 1.4015 (rough estimate)
refractive index 1.5300 (estimate)
storage temp. Refrigerator
solubility Dichloromethane, Ether, Ethyl Acetate, Methanol
pka8.08±0.20(Predicted)
form Solid
color Brown
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
MSDS Information
5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione Usage And Synthesis
Chemical PropertiesLight yellow solid
UsesQuinolinimide (cas# 4664-00-0) is a compound useful in organic synthesis.
Synthesis
Quinolinic acid

89-00-9

5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione

4664-00-0

General procedure for the synthesis of 2,3-pyridinedicarboximide from 2,3-pyridinedicarboxylic acid: 167 g of 2,3-pyridinedicarboxylic acid (1.0 mol) and 300 mL of concentrated ammonia (28%) were added to a 1000 mL three-necked flask, followed by refluxing and stirring for 6 hours at 140 °C. The reaction was carried out in a liquid mixture of 2,3-pyridinedicarboxylic acid (1.0 mol) and 300 mL of concentrated ammonia (28%). During the reaction, the liquid reaction mixture gradually changed to dark brown color. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the complete reaction of 2,3-pyridinedicarboxylic acid, the reaction mixture was cooled to room temperature. Under continuous stirring, the reaction mixture was slowly poured into 500 mL of cold water, and a large amount of gray solid precipitated immediately. The solid product was collected by filtration and the filter cake was washed with cold water and subsequently dried under vacuum at 60 °C overnight to give 125 g of gray powdery product in 84% yield.

References[1] Patent: CN102746294, 2016, B. Location in patent: Paragraph 0077; 0078
[2] Heterocycles, 2002, vol. 57, # 10, p. 1881 - 1890
[3] Bioorganic and Medicinal Chemistry, 2001, vol. 9, # 8, p. 2061 - 2071
[4] European Journal of Medicinal Chemistry, 2012, vol. 55, p. 58 - 66,9
[5] Molecules, 2000, vol. 5, # 3, p. 481 - 482
Tag:5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione(4664-00-0) Related Product Information
Pyrrolo[1,2-a]pyrazine-3-carboxylic acid (9CI) Pyrrolo1,2-apyrimidin-3-ylamine dihydrochloride Pyrrolo[1,2-a]pyrimidine-3,6-dicarboxylic acid N-Boc-6-azaindole Ethyl pyrrolo[1,2-a]pyrazine-3-carboxylate Pyrrolo1,2-apyrimidine-3,6-dicarboxylic acid 6-ethyl ester H-pyrrolo[1,2-a]pyrimidine-3-carboxylic acid 2-METHYLNICOTINALDEHYDE 3-METHYL-2-PYRIDINECARBOXALDEHYDE 2,3-Lutidine 3-(AMINOMETHYL)PYRIDINE 5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione METHYLPYRIDIN-2-YLMETHYLAMINE DIHYDROCHLORIDE 6,7-Dihydro-5H-pyrrolo[3,4-b]pyridine PYRIDINE-2-CARBOXAMIDE 3-Methylpicolinamide N-METHYLNICOTINAMIDE 3,4-PYRIDINEDICARBOXIMIDE

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