ethyl (4-acetylphenyl)carbamoylformate

Base Information

Chemical Name:ethyl (4-acetylphenyl)carbamoylformate
CAS No.:6345-12-6
Molecular Formula:C12H13 N O4
Molecular Weight:235.24
Hs Code.:2924299090
Mol file:6345-12-6.mol

Synonyms:Aceticacid, [(4-acetylphenyl)amino]oxo-, ethyl ester (9CI); Oxanilic acid,4'-acetyl-, ethyl ester (7CI); NSC 51444

Suppliers and Price of ethyl (4-acetylphenyl)carbamoylformate

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 4 raw suppliers

Chemical Property of ethyl (4-acetylphenyl)carbamoylformate

Chemical Property:

PSA：72.47000
Density:1.234g/cm³
LogP:1.46380

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of ethyl (4-acetylphenyl)carbamoylformate

There total 1 articles about ethyl (4-acetylphenyl)carbamoylformate 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:

: 99-92-3
p-aminobenzophenone

: 4755-77-5
Ethyl oxalyl chloride

: 6345-12-6
N-(4-acetyl-phenyl)-ethyl oxalate

Guidance literature:: With pyridine;

Reference yield:

: 6345-12-6
N-(4-acetyl-phenyl)-ethyl oxalate

: 17356-08-0
thiourea

: N-[4-(2-Amino-thiazol-4-yl)-phenyl]-oxalamic acid ethyl ester; hydriodide

Guidance literature:: With iodine; at 20 - 100 ℃;
DOI:10.1021/jm00362a014

Reference yield:

: 6345-12-6
N-(4-acetyl-phenyl)-ethyl oxalate

: 85849-72-5
N-{4-[4-(Ethoxyoxalyl-amino)-phenyl]-thiazol-2-yl}-oxalamic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: I₂ / 20 - 100 °C

2: pyridine / Ambient temperature

With pyridine; iodine;
DOI:10.1021/jm00362a014