30448-31-8

Basic information

• Product Name: ethyl β-anylinobutyrate
• Synonyms: ethyl β-anylinobutyrate
• CAS NO: 30448-31-8
• Molecular Weight: 207.272
• Mol File: 30448-31-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: ethyl β-anylinobutyrate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl β-anylinobutyrate(30448-31-8)
• EPA Substance Registry System: ethyl β-anylinobutyrate(30448-31-8)

Safety Data

• Hazardous Substances Data: 30448-31-8(Hazardous Substances Data)

Upstream product

• 141-97-9 ethyl acetoacetate 
• 62-53-3 aniline 
• 64-17-5 ethanol 
• 6287-35-0 ethyl 3-anilinocrotonate 
• 102879-24-3 2-methyl-N-phenylaziridine 
• 105-58-8 Diethyl carbonate 
• 6287-35-0 3-phenylaminobut-2-enoic acid ethyl ester 
• 52969-24-1 C₉H₁₂BrHgN 
• 3068-88-0 4-methyloxetan-2-one 

Downstream Products

• 81942-28-1 Phenyl-[1-(4-phenyl-furan-3-yl)-ethyl]-amine 
• 81942-16-7 3-(1-phenylvinyl)-4-methyl-1-phenylazetidine-2-one 
• 81942-13-4 methyl-3-(α-methylbenzylidene)-1-phenylazetidine-2-one 
• 81942-24-7 2-(1-anilinoethyl)-3-phenylbut-2-enolide 
• 81942-20-3 4-Methyl-1-phenyl-3-(2-phenyl-oxiranyl)-azetidin-2-one 
• 63492-84-2 3-(phenylamino)butanoic acid 
• 1258723-20-4 N-(hex-4-yn-2-yl)aniline 
• 1258723-72-6 2,5-dimethyl-6-oxo-1-phenyl-1,2,3,6-tetrahydropyridin-4-yl trifluoromethanesulfonate 
• 1258723-60-2 N-(hex-4-yn-2-yl)-N-phenylpentanamide 
• 1258723-17-9 N-(hex-4-yn-2-yl)-N-phenylacetamide 
• 1258723-64-6 N-(hex-4-yn-2-yl)-N-phenylpivalamide 
• 81942-10-1 4-methyl-1-phenylazetidine-2-one 

Relevant articles and documents

Stereodefined homopropargyl amines by tandem nucleophilic addition/fragmentation of dihydropyridone triflates

Dihydropyridone (DHPD) triflates undergo nucleophile-triggered fragmentation to provide homopropargyl amine derivatives, the stereochemistry of which is defined by starting from readily available β-amino esters.

Hydrogenation of β-N-substituted enaminoesters in the presence of ruthenium catalysts

β-Aminoesters were prepared in two simple steps from β-ketoesters derivatives and primary amines under mild conditions. Their hydrogenation was performed at 50 °C in the presence of several organometallic catalysts under acidic conditions. The new β-N-substituted aminoesters were isolated in moderate to good yields.

Hydrogenation of β-N-substituted and β-N,N-disubstituted enamino esters in the presence of iridium(I) catalyst

Several new β-amino esters were prepared in two simple steps from β-keto ester derivatives and primary and secondary amines under mild conditions. The hydrogenation of various enamino esters was performed at 50°C in the presence of iridium catalysts. The new β-N-substituted amino esters were isolated in high yields. Georg Thieme Verlag Stuttgart.