ethyl 4-[(C-ethenyl-N-tert-butyl-carbonimidoyl)amino]benzoate

Base Information Edit

Chemical Name:ethyl 4-[(C-ethenyl-N-tert-butyl-carbonimidoyl)amino]benzoate
CAS No.:73750-43-3
Molecular Formula:C16H22 N2 O2
Molecular Weight:274.35808
Hs Code.:
Mol file:73750-43-3.mol

Synonyms:Benzoicacid, 4-[[1-[(1,1-dimethylethyl)amino]-2-propenylidene]amino]-, ethyl ester(9CI); NSC 319889

Suppliers and Price of ethyl 4-[(C-ethenyl-N-tert-butyl-carbonimidoyl)amino]benzoate

Supply Marketing:Edit

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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Total 3 raw suppliers

Chemical Property of ethyl 4-[(C-ethenyl-N-tert-butyl-carbonimidoyl)amino]benzoate Edit

Chemical Property:

Vapor Pressure:9.36E-07mmHg at 25°C
Boiling Point:404.6°C at 760 mmHg
Flash Point:198.5°C
PSA：50.69000
Density:0.99g/cm³
LogP:3.73120

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of ethyl 4-[(C-ethenyl-N-tert-butyl-carbonimidoyl)amino]benzoate

There total 2 articles about ethyl 4-[(C-ethenyl-N-tert-butyl-carbonimidoyl)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: 33.0%

: N-t-butylacrylonitrilium tetrachloroferrate

: 94-09-7
p-aminoethylbenzoate

: 73750-43-3
4-[(N-tert-Butyl-acrylimidoyl)-amino]-benzoic acid ethyl ester

Guidance literature:: In dichloromethane; 1.) -70 deg C, 2.) room temperature, 15 min;

Reference yield:

: 507-20-0
tertiary butyl chloride

: 107-13-1,25014-41-9
acrylonitrile

: 94-09-7
p-aminoethylbenzoate

: 73750-43-3
4-[(N-tert-Butyl-acrylimidoyl)-amino]-benzoic acid ethyl ester

Guidance literature:: With iron(III) chloride; Yield given. Multistep reaction; 1.) dichloromethane, -40 deg C 2.) dichloromethane, -70 deg C, 15 min.;