4664-00-0

Basic information

• Product Name: QUINOLINIMIDE
• Synonyms: 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
• CAS NO: 4664-00-0
• Molecular Formula: C₇H₄N₂O₂
• Molecular Weight: 148.12
• EINECS: 225-107-1
• Product Categories: Pyridine;Miscellaneous Reagents;Aromatics;Heterocycles;Heterocycle-Pyridine series
• Mol File: 4664-00-0.mol
• Article Data: 17

Chemical Properties

• Melting Point: 233-234°C
• Boiling Point: 268.69°C (rough estimate)
• Appearance: Light yellow solid
• 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)
• CAS DataBase Reference: QUINOLINIMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: QUINOLINIMIDE(4664-00-0)
• EPA Substance Registry System: QUINOLINIMIDE(4664-00-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39
• Hazardous Substances Data: 4664-00-0(Hazardous Substances Data)

Usage

Chemical Properties

Light yellow solid

Uses

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

InChI:InChI=1/C7H4N2O2/c10-6-4-1-2-8-3-5(4)7(11)9-6/h1-3H,(H,9,10,11)

Upstream product

• 60-35-5 acetamide 
• 699-98-9 Pyridine-2,3-dicarboxylic anhydride 
• 57-13-6 urea 
• 89-00-9 Pyridine-2,3-dicarboxylic acid 
• 4663-94-9 pyridine-2,3-dicarboxamide 
• 108-24-7 acetic anhydride 
• 73112-09-1 2-cyanopyridine-3-carboxylic acid 

Downstream Products

• 120347-89-9 6-benzyl-6,7-dihydro-7-hydroxypyrrolo<3,4-b>pyridin-5-one 
• 18184-75-3 6-benzyl-5H-pyrrolo[3,4-b]pyridine-5,7(6H)-dione 
• 442882-27-1 6-(4-methoxybenzyl)-5H-pyrrolo[3,4-b]pyridine-5,7(6H)-dione 
• 158060-81-2 2,8-diazabicyclo[4.3.0]nonane 
• 128740-14-7 (R,R)-8-benzyl-2,8-diazabicyclo[4.3.0]-nonane 
• 5654-94-4 2,8-diazabicyclo-[4.3.0]-nonane 
• 6789-51-1 6-methyl-5H-pyrrolo[3,4-b]pyridine-5,7(6H)-dione 
• 40107-93-5 6,7-dihydro-5H-pyrrolo<3,4-b>pyridin-5-one 
• 1395044-59-3 methyl 2-((methoxycarbonyl)amino)pyridinecarboxylate 
• 107468-56-4 methyl 3-((methoxycarbonyl)amino)picolinate 
• 860299-07-6 2-(5,7-dioxo-5,7-dihydro-pyrrolo[3,4-b]pyridin-6-yl)-N-methyl-N-phenyl-acetamide 
• 88332-13-2 N-n-butylpyridyl-2,3-dicarboximide 

Relevant articles and documents

Method for preparing 6,7-dihydro-5H-pyrrolo-pyridine hydrochloride

The invention discloses a preparation method for preparing 6,7-dihydro-5H-pyrrolo-pyridine hydrochloride. The method is characterized in that a target product 6,7-dihydro-5H-pyrrolo-pyridine hydrochloride is obtained through lactamization, reduction and salifying by taking furo[3,4-b]pyridine-5,7-dione as an original raw material. The compound is an important medical intermediate.

Pyridine salt / 1,4-dihydropyridine derivative and preparation method thereof

The present invention discloses a pyridine salt / 1,4-dihydropyridine derivative (NAD / NADH analog) with novel structure. The NAD / NADH analog can substitute natural NAD / NADH to be applied to a biochemical system for redox reactions, and can also be used as an electron carrier for the energy transfer of an enzymatic fuel cell. Further, the NAD / NADH analogs provided by the invention are easy to prepare, isolate and purify, and have a high yield.

New artificial fluoro-cofactor of hydride transfer with novel fluorescence assay for redox biocatalysis

A new artificial fluoro-cofactor was developed for the replacement of natural cofactors NAD(P), exhibiting a high hydride transfer ability. More importantly, we established a new and fast screening method for the evaluation of the properties of artificial cofactors based on the fluorescence assay and visible color change.