883251-16-9

Basic information

• Product Name: 6-benzyloxy-7-methoxy-2-methylquinoline-3-carboxylic acid
• Synonyms: 6-benzyloxy-7-methoxy-2-methylquinoline-3-carboxylic acid
• CAS NO: 883251-16-9
• Molecular Weight: 323.348
• Mol File: 883251-16-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 6-benzyloxy-7-methoxy-2-methylquinoline-3-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 6-benzyloxy-7-methoxy-2-methylquinoline-3-carboxylic acid(883251-16-9)
• EPA Substance Registry System: 6-benzyloxy-7-methoxy-2-methylquinoline-3-carboxylic acid(883251-16-9)

Safety Data

• Hazardous Substances Data: 883251-16-9(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 1042978-66-4 5-benzyloxy-4-methoxy-2-aminobenzaldehyde 
• 141-97-9 ethyl acetoacetate 
• 621-59-0 isovanillin 
• 6346-05-0 3-benzyloxy-4-methoxybenzaldehyde 
• 58662-50-3 2-aldehyde-4-benzyloxy-5-methoxy nitrobenzene 
• 883251-13-6 ethyl 6-benzyloxy-7-methoxy-2-methylquinoline-3-carboxylate 

Downstream Products

• 1426814-47-2 6-benzyloxy-7-methoxy-2-methyl-N-(2-(thiophen-2-yl)ethyl)quinoline-3-carboxamide 
• 1427216-11-2 6-(benzyloxy)-7-methoxy-2-methyl-N-(4-methylphenyl)quinoline-3-carboxamide 
• 1426813-87-7 6-benzyloxy-7-methoxy-2-methyl-N-(n-pentyl)quinoline-3-carboxamide 
• 1426814-28-9 6-benzyloxy-7-methoxy-2-methyl-N-(tert-butyl)quinoline-3-carboxamide 
• 1426813-91-3 6-(benzyloxy)-7-methoxy-2-methyl-N-(benzyl)quinoline-3-carboxamide 
• 883251-21-6 N-(1-hydroxymethyl-2-phenylethyl)-6-benzyloxy-7-methoxy-2-methylquinoline-3-carboxamide 
• 883251-40-9 N-(1-hydroxymethyl-2-phenylethyl)-6-hydroxy-7-methoxy-2-methylquinoline-3-carboxamide 

Relevant articles and documents

Quinoline-3-carboxamide derivatives as potential cholesteryl ester transfer protein inhibitors

A series of novel quinoline-3-carboxamide derivatives 10-17 and 23-27 were designed and synthesized as cholesteryl ester transfer protein (CETP) inhibitors. All of them exhibited activity against CETP. Particularly, compounds 24 and 26 displayed the best activity against CETP with the same inhibitory rate of 80.1%.