108763-28-6

Basic information

• Product Name: 6-Quinoxalinecarboxaldehyde,2,3-dimethyl-(9CI)
• Synonyms: 6-Quinoxalinecarboxaldehyde,2,3-dimethyl-(9CI);2,3-DIMETHYLQUINOXALINE-6-CARBALDEHYDE
• CAS NO: 108763-28-6
• Molecular Formula: C11 H10 N2 O
• Molecular Weight: 0
• Product Categories: PIPERIDINE
• Mol File: 108763-28-6.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-Quinoxalinecarboxaldehyde,2,3-dimethyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Quinoxalinecarboxaldehyde,2,3-dimethyl-(9CI)(108763-28-6)
• EPA Substance Registry System: 6-Quinoxalinecarboxaldehyde,2,3-dimethyl-(9CI)(108763-28-6)

Safety Data

• Hazardous Substances Data: 108763-28-6(Hazardous Substances Data)

Upstream product

• 65833-70-7 (2,3-dimethylquinoxalin-6-yl)methanol 
• 1313-13-9 manganese dioxide 
• 619-05-6 3,4-diaminobenzoic acid 
• 17635-26-6 2,3-dimethyl-6-quinoxalinecarboxylic acid 

Downstream Products

• 1334764-15-6 3-{2-[4-(2,3-dimethylquinoxalin-6-yl)-3-(6-methylpyridin-2-yl)-1H-pyrazol-1-yl]acetamido}benzamide 
• 1334764-11-2 N-(3-cyanophenyl)-2-[4-(2,3-dimethylquinoxalin-6-yl)-3-(6-methylpyridin-2-yl)-1H-pyrazol-1-yl]ethanethioamide 
• 1334764-07-6 2-[4-(2,3-dimethylquinoxalin-6-yl)-3-(6-methylpyridin-2-yl)-1H-pyrazol-1-yl]-N-phenylethanethioamide 
• 1334764-03-2 N-(3-cyanophenyl)-3-[4-(2,3-dimethylquinoxalin-6-yl)-3-(6-methylpyridin-2-yl)-1H-pyrazol-1-yl]propanamide 
• 1334763-96-0 N-(3-cyanophenyl)-2-[4-(2,3-dimethylquinoxalin-6-yl)-3-(6-methylpyridin-2-yl)-1H-pyrazol-1-yl]acetamide 
• 1334763-98-2 N-(3-cyanophenyl)-2-[4-(2,3-dimethylquinoxalin-6-yl)-5-(6-methylpyridin-2-yl)-1H-pyrazol-1-yl]acetamide 

Relevant articles and documents

A new family of quinoline and quinoxaline analogues of combretastatins

The 3-hydroxy-4-methoxyphenyl ring of combretastatin A-4 can be replaced by a 2-naphthyl moiety without significant loss of cytotoxicity and inhibition of tubulin polymerization potency. In this paper we show that the 6- or 7-quinolyl systems can in turn replace both cyclic moieties, keeping in the first case most of the potency as cytotoxic agent and in the second case as inhibitor of tubulin polymerization, related to the activities displayed by model compounds.