ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Pyridine compound >Pyridine derivatives >5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione

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

5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione Structure
CAS No.
4664-00-0
Chemical Name:
5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione
Synonyms
NSC 405554;AKOS 93366;QUINOLINIMIDE;3-azaphthalimid;Moxifloxacin Imp.X;QUINOLINICACIDAMIDE;quinolinicacidimide;pyridinedicarboxamide;2,3-Pyridinedicarbimide;Pyridine-2,3-dicarbimide
CBNumber:
CB4463896
Molecular Formula:
C7H4N2O2
Molecular Weight:
148.12
MOL File:
4664-00-0.mol
MSDS File:
SDS
Modify Date:
2023/4/23 13:52:06

5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione 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
pka 8.08±0.20(Predicted)
form Solid
color Brown

SAFETY

Risk and Safety Statements

Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-37/39

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

Chemical Properties

Light yellow solid

Uses

Quinolinimide (cas# 4664-00-0) is a compound useful in organic synthesis.

5H-Pyrrolo[3,4-b]pyridine-5,7(6H)-dione Preparation Products And Raw materials

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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 AKOS 93366 5H-PYRROLO[3,4-B]PYRIDINE-5,7(6H)-DIONE QUINOLINIMIDE PYRROLO[3,4-B]PYRIDINE-5,7-DIONE 2,3-pyridinedicarboximide 3-azaphthalimid pyridinedicarboxamide quinolinicacidimide 3-Azaphthalimid [German] 5H-Pyrrolo(3,4-b)pyridine-5,7(6H)-dione (9CI) pyrrolo[3,4-b]pyridine-5,7-quinone 2,3-Pyridinedicarboximide(WX619013) Moxifloxacin Imp.X QUINOLINIMIDE ISO 9001:2015 REACH 2,3-pyridinedicarboximidequinolinimide 4664-00-0 Heterocycle-Pyridine series Pyridine Miscellaneous Reagents Aromatics Heterocycles