535969-70-1

Basic information

• Product Name: 3-Quinolinecarboxamide, N-(3,5-difluorophenyl)-1-(3,5-dimethoxyphenyl)-N-ethyl-1,4-dihydro-4-ox o-7-(phenylmethoxy)-
• CAS NO: 535969-70-1
• Molecular Formula: C33H28F2N2O5
• Molecular Weight: 570.593
• Mol File: 535969-70-1.mol

Chemical Properties

• CAS DataBase Reference: 3-Quinolinecarboxamide, N-(3,5-difluorophenyl)-1-(3,5-dimethoxyphenyl)-N-ethyl-1,4-dihydro-4-ox o-7-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Quinolinecarboxamide, N-(3,5-difluorophenyl)-1-(3,5-dimethoxyphenyl)-N-ethyl-1,4-dihydro-4-ox o-7-(phenylmethoxy)-(535969-70-1)
• EPA Substance Registry System: 3-Quinolinecarboxamide, N-(3,5-difluorophenyl)-1-(3,5-dimethoxyphenyl)-N-ethyl-1,4-dihydro-4-ox o-7-(phenylmethoxy)-(535969-70-1)

Safety Data

• Hazardous Substances Data: 535969-70-1(Hazardous Substances Data)

Upstream product

• 119284-23-0 N-ethyl-3,5-difluoroaniline 

Downstream Products

• 535969-71-2 1-(3,5-dimethoxy-phenyl)-7-hydroxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (3,5-difluoro-phenyl)-ethyl-amide 
• 535969-81-4 7-(8-bromo-octyloxy)-1-(3,5-dimethoxy-phenyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (3,5-difluoro-phenyl)-ethyl-amide 
• 535969-73-4 7-(7-bromo-heptyloxy)-1-(3,5-dimethoxy-phenyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (3,5-difluoro-phenyl)-ethyl-amide 
• 535969-79-0 1-(3,5-dimethoxy-phenyl)-7-(6-iodo-hexyloxy)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (3,5-difluoro-phenyl)-ethyl-amide 
• 535969-75-6 7-(4-chloromethyl-benzyloxy)-1-(3,5-dimethoxy-phenyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (3,5-difluoro-phenyl)-ethyl-amide 
• 535969-77-8 1-(3,5-dimethoxy-phenyl)-7-(5-iodo-pentyloxy)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (3,5-difluoro-phenyl)-ethyl-amide 

Relevant articles and documents

A novel class of apical sodium-dependent bile acid transporter inhibitors: The amphiphilic 4-oxo-1-phenyl-1,4-dihydroquinoline derivatives

A series of 4-oxo-1-phenyl-1,4-dihydroquinolines possessing a linker and an ammonio moiety were synthesized and found to inhibit the apical sodium-dependent bile acid transporter (ASBT). The potency of ASBT inhibition varied with the position and length o