Carbamic acid, bis(phenylmethyl)-, ethyl ester

Base Information

Chemical Name:Carbamic acid, bis(phenylmethyl)-, ethyl ester
CAS No.:101584-40-1
Molecular Formula:C17H19NO2
Molecular Weight:269.33800
Hs Code.:
Mol file:101584-40-1.mol

Synonyms:Dibenzyl-carbamidsaeure-aethylester;Dibenzylurethan;dibenzyl-carbamic acid ethyl ester;ethoxy-N,N-bisbenzylcarboxamide;ethyl dibenzylcarbamate;Carbamic acid,bis(phenylmethyl)-,ethyl ester;

Suppliers and Price of Carbamic acid, bis(phenylmethyl)-, ethyl ester

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
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price

Total 1 raw suppliers

Chemical Property of Carbamic acid, bis(phenylmethyl)-, ethyl ester

Chemical Property:

PSA：29.54000
LogP:3.84530

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Carbamic acid, bis(phenylmethyl)-, ethyl ester

There total 4 articles about Carbamic acid, bis(phenylmethyl)-, ethyl ester 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: 90.0%

: 541-41-3
chloroformic acid ethyl ester

: 103-49-1
dibenzylamine

: 101584-40-1
ethyl dibenzylcarbamate

Guidance literature:: In tetrahydrofuran; water; acetone; at 0 - 20 ℃; for 2h;
DOI:10.1002/adsc.201600654

Reference yield:

: 124-38-9,18923-20-1
carbon dioxide

: 75-03-6
ethyl iodide

: 103-49-1
dibenzylamine

: 101584-40-1
ethyl dibenzylcarbamate

Guidance literature:: With oxygen; tetraethylammonium perchlorate; Yield given. Multistep reaction; 1.) -1.0 V vs SCE, MeCN, 2.) 60 min, 3.) room temperature, overnight;
DOI:10.1021/jo970308h