854770-54-0

Basic information

• Product Name: Phenol, 3-[3-methyl-8-(trifluoromethyl)-4-quinolinyl]-
• CAS NO: 854770-54-0
• Molecular Formula: C17H12F3NO
• Molecular Weight: 303.284
• Mol File: 854770-54-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Phenol, 3-[3-methyl-8-(trifluoromethyl)-4-quinolinyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 3-[3-methyl-8-(trifluoromethyl)-4-quinolinyl]-(854770-54-0)
• EPA Substance Registry System: Phenol, 3-[3-methyl-8-(trifluoromethyl)-4-quinolinyl]-(854770-54-0)

Safety Data

• Hazardous Substances Data: 854770-54-0(Hazardous Substances Data)

Upstream product

• 854778-41-9 [2-amino-3-(trifluoro-methyl)phenyl](3-hydroxyphenyl)methanone 
• 123-38-6 propionaldehyde 

Downstream Products

• 1020736-50-8 3,5-dichloro-2-fluoro-6-{3-[3-methyl-8-(trifluoromethyl)quinolin-4-yl]phenoxy}pyridin-4-amine 
• 1020736-31-5 4-[3-(6-fluoro-pyridin-2-yloxy)-phenyl]-3-methyl-8-trifluoromethyl-quinoline 
• 1020736-40-6 3-methyl-4-(3-{[5-(methylsulfonyl)pyridin-3-yl]oxy}phenyl)-8-(trifluoromethyl)quinoline 
• 1020735-54-9 4-{3-[4-methoxy-3-(methylsulfonyl)phenoxy]phenyl}-3-methyl-8-(trifluoromethyl)quinoline 
• 1020735-40-3 4-{3-[4-methyl-3-(methylsulfonyl)phenoxy]phenyl}-8-(trifluoromethyl)quinoline 
• 1020736-34-8 3-methyl-4-[3-(4-methylsulfanyl-pyridin-2-yloxy)-phenyl]-8-trifluoromethyl-quinoline 
• 1020736-47-3 4-[3-(4,6-dichloro-1-oxy-pyridin-2-yloxy)-phenyl]-3-methyl-8-trifluoromethyl-quinoline 
• 1020734-73-9 4-{3-[3-(ethylsulfonyl)phenoxy]phenyl}-3-methyl-8-(trifluoromethyl)quinoline 
• 1020736-41-7 3-methyl-4-[3-(2-methylsulfanyl-pyridin-4-yloxy)-phenyl]-8-trifluoromethyl-quinoline 
• 854775-66-9 methyl 3-{3-[3-methyl-8-(trifluoromethyl)quinolin-4-yl]phenoxy}benzoate 
• 854775-67-0 methyl 4-{3-[3-methyl-8-(trifluoromethyl)quinolin-4-yl]phenoxy}benzoate 
• 1354628-53-7 3-[3-methyl-8-(trifluoromethyl)quinolin-4-yl]phenyl 3-(methylsulfonyl)benzoate 

Relevant articles and documents

4-(3-Aryloxyaryl)quinoline alcohols are liver X receptor agonists

A series of 4-(3-aryloxyaryl)quinolines with alcohol substituents on the terminal aryl ring was prepared as potential LXR agonists, in which an alcohol group replaced an amide in previously reported amide analogs. High affinity LXR ligands with excellent