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14891-08-8

14891-08-8 Structure

14891-08-8 Structure
IdentificationBack Directory
[Name]

N-(ETHOXYCARBONYL)-N-(ETHOXYCARBONYKLETHYL)GLYCINE ETHYL ESTER
[CAS]

14891-08-8
[Synonyms]

N,N-bis[2-(1,3-dioxolan-2-yl)ethyl]
N-(Ethoxycarbonyl)-N-(ethoxycarbonylethyl)glycine ethyl ester
ethyl 3-[ethoxycarbonyl-(2-ethoxy-2-oxoethyl)amino]propanoate
ETHYL 3-((2-ETHOXY-2-OXOETHYL)(ETHOXYCARBONYL)AMINO)PROPANOATE
N-(ETHOXYCARBONYL)-N-(ETHOXYCARBONYKLETHYL)GLYCINE ETHYL ESTER
N-(Ethoxycarbonyl)-N-(2-ethoxy-2-oxoethyl)-alanine ethyl ester
ETHYL N-(ETHOXYCARBONYL)-N-(ETHOXYCARBONYLMETHYL)-3-AMINOPROPIONATE
β-Alanine, N-(ethoxycarbonyl)-N-(2-ethoxy-2-oxoethyl)-, ethyl ester
[Molecular Formula]

C12H21NO6
[MDL Number]

MFCD00027803
[MOL File]

14891-08-8.mol
[Molecular Weight]

275.3
Raw materials And Preparation ProductsBack Directory
Safety DataBack Directory
[HS Code ]

2924190090
Hazard InformationBack Directory
[Chemical Properties]

liquid. Boiling point 155-166℃/0.40kPa.
[Uses]

N-(Ethoxycarbonyl)-N-(ethoxycarbonylethyl)glycine ethyl ester can be used for an intermediate of the hydrobromate of pumpkin seed.
[Synthesis]

Addition of glycine and acrylonitrile to generate N-cyanoethylglycine, which is then esterified with ethanol under acid catalysis to obtain N-(ethoxycarbonylethyl)glycine ethyl ester hydrochloride, which is combined with ethyl chloroformate .N-(Ethoxycarbonyl)-N-(ethoxycarbonylethyl)glycine ethyl ester is obtained by condensation with the participation of sodium carbonate.
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