30130-96-2

Basic information

• Product Name: Propanoic acid, 3-[(2-ethoxy-2-oxoethyl)(phenylmethyl)amino]-3-oxo-, ethyl ester
• CAS NO: 30130-96-2
• Molecular Formula: C16H21NO5
• Molecular Weight: 307.346
• Mol File: 30130-96-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Propanoic acid, 3-[(2-ethoxy-2-oxoethyl)(phenylmethyl)amino]-3-oxo-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanoic acid, 3-[(2-ethoxy-2-oxoethyl)(phenylmethyl)amino]-3-oxo-, ethyl ester(30130-96-2)
• EPA Substance Registry System: Propanoic acid, 3-[(2-ethoxy-2-oxoethyl)(phenylmethyl)amino]-3-oxo-, ethyl ester(30130-96-2)

Safety Data

• Hazardous Substances Data: 30130-96-2(Hazardous Substances Data)

Upstream product

• 100-46-9 benzylamine 
• 1071-46-1 hydrogen ethyl malonate 
• 6436-90-4 ethyl 2-(benzylamino)acetate 
• 36239-09-5 ethyl chlorocarbonylacetate 

Downstream Products

• 67513-35-3 ethyl 1-benzyl-4-hydroxy-3-pyrrolin-2-one-3-carboxylate 
• 105776-64-5 methyl 7-benzyl-3,6-dioxo-2-phenyl-1,2,3,6,7,8-hexahydropyrazolo<3,4-c>azepine-4-carboxylate 
• 105776-98-5 dimethyl 1-benzyl-6-(pyrrolidin-1'-yl)-2-oxo-2,7-dihydro-1H-azepine-4,5-dicarboxylate 
• 105776-96-3 1-benzyl-4-hydroxy-3-(1'-benzyl-5'-oxo-3'-pyrrolin-3'-yl)-3-pyrrolin-2-one 
• 105776-58-7 dimethyl 1-benzyl-6-hydroxy-2-oxo-2,3,4,7-tetrahydro-1H-azepine-4,5-dicarboxylate 
• 105776-59-8 dimethyl 1-benzyl-6-methoxy-2-oxo-2,7-dihydro-1H-azepine-4,5-dicarboxylate 
• 105776-63-4 methyl 7-benzyl-3,6-dioxo-1,2,3,6,7,8-hexahydropyrazolo<3,4-c>azepine-4-carboxylate 
• 105776-57-6 dimethyl 1-benzyl-6-hydroxy-2-oxo-2,7-dihydro-1H-azepine-4,5-dicarboxylate 
• 105776-92-9 1-benzyl-4-(pyrrolidin-1'-yl)-3-pyrrolin-2-one 
• 30125-76-9 1-(phenylmethyl)pyrrolidine-2,4-dione 
• 154669-34-8 1-Benzyl-3-diazo-2,4-pyrrolidindion 
• 87259-92-5 N-benzylstaurosporinone 
• 501417-98-7 Methyl-1-benzyl-3-methyl-2,4-dioxo pyrrolidine-3-carboxylate 
• 501417-91-0 methyl N-benzylpyrrolidin-2,4-dione 3-carboxylate 

Relevant articles and documents

Facile access to 3-alkyl-substituted 3-hydroperoxy-2,4-pyrrolidinediones using manganese(III)-catalyzed aerobic oxidation

3-Alkyl-substituted 2,4-pyrrolidinediones were directly oxidized under very mild manganese(III)-catalyzed aerobic oxidation conditions to give the corresponding 3-hydroperoxy-2,4-pyrrolidinediones in quantitative yields. The scope and limitations for the

Design and implementation of an efficient synthetic approach to furanosylated indolocarbazoles: Total synthesis of (+)- and (-)-K252a

The first total synthesis of the natural product (+)-K252a (2) has been achieved in 12 steps from commercially available materials, with a longest linear sequence of seven steps and an overall yield of 21%. The synthetic strategy employs novel rhodium carbenoid chemistry in the construction of both the indolocarbazole aglycon (4) and the carbohydrate moiety (9).