1040735-65-6

Basic information

• Product Name: ethyl 2-(2-ethoxycarbonylethyl)-3-oxocyclohexenebutyrate
• Synonyms: ethyl 2-(2-ethoxycarbonylethyl)-3-oxocyclohexenebutyrate
• CAS NO: 1040735-65-6
• Molecular Weight: 310.39
• Mol File: 1040735-65-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: ethyl 2-(2-ethoxycarbonylethyl)-3-oxocyclohexenebutyrate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(2-ethoxycarbonylethyl)-3-oxocyclohexenebutyrate(1040735-65-6)
• EPA Substance Registry System: ethyl 2-(2-ethoxycarbonylethyl)-3-oxocyclohexenebutyrate(1040735-65-6)

Safety Data

• Hazardous Substances Data: 1040735-65-6(Hazardous Substances Data)

Upstream product

• 1040735-62-3 diethyl 5,9-dioxotridecanedioate 
• 56613-80-0 D-2-phenylglycinol 
• 54135-60-3 2,2'-methylenebis(cyclohexane-1,3-dione) 
• 64-17-5 ethanol 

Downstream Products

• 1040735-63-4 ethyl (3R,7aS,11aS)-5-oxo-3-phenyl-2,3,5,6,7,7a,10,11-octahydrooxazolo[2,3-j]quinoline-8-butyrate 
• 1040735-87-2 ethyl (3R,7aR,11aR)-5-oxo-3-phenyl-2,3,5,6,7,7a,10,11-octahydrooxazolo[2,3-j]quinoline-8-butyrate 

Relevant articles and documents

Biomimetic construction of the hydroquinoline ring system. Diastereodivergent enantioselective synthesis of 2,5-disubstituted cis -decahydroquinolines

Figure presented The straightforward enantioselective construction of the hydroquinoline ring system from 1,5-polycarbonyl derivatives, using (R)-phenyglycinol as a chiral latent form of ammonia, is reported. The process mimics the key steps believed to o