Ethyl alpha-amino-4-(2-ethoxy-2-oxoethyl)cyclohexanepropanoate

Base Information

Chemical Name:Ethyl alpha-amino-4-(2-ethoxy-2-oxoethyl)cyclohexanepropanoate
CAS No.:156143-93-0
Molecular Formula:C₁₅H₂₇NO₄
Molecular Weight:285.384
Hs Code.:
DSSTox Substance ID:DTXSID301194613

Synonyms:DTXSID301194613;Ethyl alpha-amino-4-(2-ethoxy-2-oxoethyl)cyclohexanepropanoate;156143-93-0

Suppliers and Price of Ethyl alpha-amino-4-(2-ethoxy-2-oxoethyl)cyclohexanepropanoate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of Ethyl alpha-amino-4-(2-ethoxy-2-oxoethyl)cyclohexanepropanoate

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:9
Exact Mass:285.19400834
Heavy Atom Count:20
Complexity:311

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)CC1CCC(CC1)CC(C(=O)OCC)N

Technology Process of Ethyl alpha-amino-4-(2-ethoxy-2-oxoethyl)cyclohexanepropanoate

There total 3 articles about Ethyl alpha-amino-4-(2-ethoxy-2-oxoethyl)cyclohexanepropanoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: 156143-77-0
2-Amino-3-(4-ethoxycarbonylmethyl-phenyl)-propionic acid ethyl ester

: 156143-93-0
2-Amino-3-(4-ethoxycarbonylmethyl-cyclohexyl)-propionic acid ethyl ester

Guidance literature:: With hydrogen; acetic acid; platinum(IV) oxide; at 80 ℃; under 60004.8 Torr;
DOI:10.1021/jm00035a014

Reference yield:

: 7398-81-4
(4-bromomethylphenyl)acetic acid ethyl ester

: 156143-93-0
2-Amino-3-(4-ethoxycarbonylmethyl-cyclohexyl)-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 79 percent / KI, benzyltrimethylammonium hydroxide / dioxane; H₂O / 3 h / Ambient temperature

2: 83 percent / 1 N aq. HCl / diethyl ether / 4 h / Ambient temperature

3: 100 percent / H₂, 80percent aq. AcOH / PtO₂ / 80 °C / 60004.8 Torr

With hydrogenchloride; hydrogen; N-benzyl-trimethylammonium hydroxide; acetic acid; potassium iodide; platinum(IV) oxide; In 1,4-dioxane; diethyl ether; water;
DOI:10.1021/jm00035a014

Reference yield:

: 156143-76-9
2-(Benzhydrylidene-amino)-3-(4-ethoxycarbonylmethyl-phenyl)-propionic acid ethyl ester

: 156143-93-0
2-Amino-3-(4-ethoxycarbonylmethyl-cyclohexyl)-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / 1 N aq. HCl / diethyl ether / 4 h / Ambient temperature

2: 100 percent / H₂, 80percent aq. AcOH / PtO₂ / 80 °C / 60004.8 Torr

With hydrogenchloride; hydrogen; acetic acid; platinum(IV) oxide; In diethyl ether;
DOI:10.1021/jm00035a014