141750-56-3

Basic information

• Product Name: (E)-3-[2-cyclopropyl-4-(4-fluoro-phenyl)-quinolin-3-yl]-N-methoxy-N-methyl-acrylamide
• Synonyms: (E)-3-[2-cyclopropyl-4-(4-fluoro-phenyl)-quinolin-3-yl]-N-methoxy-N-methyl-acrylamide
• CAS NO: 141750-56-3
• Molecular Weight: 376.43
• Mol File: 141750-56-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-3-[2-cyclopropyl-4-(4-fluoro-phenyl)-quinolin-3-yl]-N-methoxy-N-methyl-acrylamide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-[2-cyclopropyl-4-(4-fluoro-phenyl)-quinolin-3-yl]-N-methoxy-N-methyl-acrylamide(141750-56-3)
• EPA Substance Registry System: (E)-3-[2-cyclopropyl-4-(4-fluoro-phenyl)-quinolin-3-yl]-N-methoxy-N-methyl-acrylamide(141750-56-3)

Safety Data

• Hazardous Substances Data: 141750-56-3(Hazardous Substances Data)

Upstream product

• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 
• 222306-21-0 (E)-3-[2-cyclopropyl-4-(4-fluoro-phenyl)-quinolin-3-yl]-acrylic acid 
• 124-63-0 methanesulfonyl chloride 
• 155849-96-0 N-methoxy-N-methyl3-<2-cyclopropyl-4-(4-fluorophenyl)quinolin-2-yl>-3-hydroxypropanamide 
• 124931-12-0 diethyl (N-methoxy-N-methylcarbamoylmethyl)phosphonate 
• 121660-37-5 2-cyclopropyl-4-(4-fluorophenyl)-3-formylquinoline 

Downstream Products

• 141750-57-4 (4R)-4,7,7-trimethyl-3-exo-(1-naphthyl)bicyclo<2.2.1>heptan-2-exo-yl (E)-7-<2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl>-3,5-dioxo-6-heptenoate 
• 634920-21-1 (S)-(E)-7-[2-Cyclopropyl-4-(4-fluoro-phenyl)-quinolin-3-yl]-3,5-dioxo-hept-6-enoic acid phenylethyl amide 
• 166803-31-2 (E)-7-[2-cyclopropyl-4-(4-fluoro-phenyl)-quinolin-3-yl]-3,5-dioxo-hept-6-enoic acid ethyl ester 

Relevant articles and documents

Process for the manufacture of organic compounds

The invention relates to a process for the manufacture of a compound of formula or a salt, especially a pharmaceutically acceptable salt with a base, thereof or a lactone thereof wherein the element represents —CH2—CH2— or —CH═CH— an

Optically active esters of 7-substituted 3,5-difunctionalized 6-heptenoic acids

The present invention provides optically active esters of 7-substituted 3,5-difunctionalized 6-heptenoic acids represented by the following formula: STR1 wherein R is a substituted or unsubstituted aromatic group, a substituted or unsubstituted heteroarom