ethyl 3-amino-4-[2-(1,3-dioxoisoindol-2-yl)ethoxy]but-2-enoate - Names and Identifiers
Name | Ethyl 3-amino-4-(2-phthalimidoethoxy)crotonate
|
Synonyms | OEBFVKDPQVFAPH-UHFFFAOYSA-N Ethyl 3-amino-4-(2-phthalimidoethoxy)crotonate ETHYL3-AMINO-4-(2-PHTHALIMIDOETHOXY)-CROTONATE Ethyl 3-amino-4-(2,2-diethoxy-ethoxy)crotonate 3-amino-4-(2,2-diethoxy-ethoxy)-but-2-cnoic acid ethyl ester ethyl 3-amino-4-[2-(1,3-dioxoisoindol-2-yl)ethoxy]but-2-enoate Ethyl 3-aMino-4-(2-(1,3-dioxoisoindolin-2-yl)ethoxy)but-2-enoate (Z)-Ethyl 3-amino-4-(2-(1,3-dioxoisoindolin-2-yl)ethoxy)but-2-enoate ethyl (2Z)-3-amino-4-[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethoxy]but-2-enoate 2-Butenoic acid, 3-amino-4-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethoxy]-, ethyl ester
|
CAS | 265136-65-0
|
InChI | InChI=1/C16H18N2O5/c1-2-23-14(19)9-11(17)10-22-8-7-18-15(20)12-5-3-4-6-13(12)16(18)21/h3-6,9H,2,7-8,10,17H2,1H3/b11-9- |
ethyl 3-amino-4-[2-(1,3-dioxoisoindol-2-yl)ethoxy]but-2-enoate - Physico-chemical Properties
Molecular Formula | C16H18N2O5
|
Molar Mass | 318.32 |
Density | 1.293±0.06 g/cm3(Predicted) |
Melting Point | 88-90 °C |
Boling Point | 502.5±50.0 °C(Predicted) |
Flash Point | 257.7°C |
Vapor Presure | 3.16E-10mmHg at 25°C |
pKa | 3.91±0.70(Predicted) |
Refractive Index | 1.578 |
ethyl 3-amino-4-[2-(1,3-dioxoisoindol-2-yl)ethoxy]but-2-enoate - Introduction
Ethyl 3-amino-4-(2-phthalimidoethoxy)crotonate is an organic compound with the chemical formula C16H16N2O5.
Nature:
Ethyl 3-amino-4-(2-phthalimidoethoxy)crotonate is a white or pale yellow crystalline solid. It is insoluble in water at room temperature, but soluble in many organic solvents, such as chloroform, ether and dichloromethane. It has a melting point of 136 ° C.
Use:
Ethyl 3-amino-4-(2-phthalimidoethoxy)crotonate is a commonly used intermediate compound that plays an important role in organic synthesis. It can be used to synthesize other organic substances, such as drugs, dyes and polymers.
Method:
Ethyl 3-amino-4-(2-phthalimidoethoxy)crotonate can be synthesized by various methods. One of the commonly used methods is to react benzyl chloromethyl Ethyl ketone with phthalic anhydride to obtain Ethyl phthalate, it is then reacted with β-amine ethanol to form the desired product.
Safety Information:
The toxicity and danger of Ethyl 3-amino-4-(2-phthalimidoethoxy)crotonate have not been studied in detail, so it is necessary to pay attention to safe operation when using it. Wear appropriate personal protective equipment when handling this compound to avoid direct skin contact or inhalation of its volatiles. In the use, storage and disposal, should strictly follow the chemical safety procedures.
Last Update:2024-04-09 19:05:48