Methyl 3-[(3-ethoxyacryloyl)amino]benzoate

Base Information

Chemical Name:Methyl 3-[(3-ethoxyacryloyl)amino]benzoate
CAS No.:88371-31-7
Molecular Formula:C13H15NO4
Molecular Weight:249.266
Hs Code.:
DSSTox Substance ID:DTXSID90707834

Synonyms:88371-31-7;Methyl 3-[(3-ethoxyacryloyl)amino]benzoate;DTXSID90707834;IXLZDUYBUURIQH-UHFFFAOYSA-N;m-methoxycarbonyl-N-(beta-ethoxyacryloyl)aniline

Suppliers and Price of Methyl 3-[(3-ethoxyacryloyl)amino]benzoate

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 Methyl 3-[(3-ethoxyacryloyl)amino]benzoate

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:249.10010796
Heavy Atom Count:18
Complexity:314

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC=CC(=O)NC1=CC=CC(=C1)C(=O)OC

Technology Process of Methyl 3-[(3-ethoxyacryloyl)amino]benzoate

There total 3 articles about Methyl 3-[(3-ethoxyacryloyl)amino]benzoate 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: 59.0%

: 4518-10-9
Methyl 3-aminobenzoate

: 6191-99-7
3-ethoxyacryloyl chloride

: 88371-31-7
C₁₃H₁₅NO₄

Guidance literature:: With pyridine; In dichloromethane; at 0 - 20 ℃; for 2.5h; Inert atmosphere;

Reference yield:

: 99-05-8,159139-79-4
meta-aminobenzoic acid

: 88371-31-7
C₁₃H₁₅NO₄

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride

2: pyridine / dichloromethane

With pyridine; thionyl chloride; In dichloromethane;
DOI:10.1016/j.bioorg.2011.07.001