Ethyl (2-oxo-2-phenylethyl)carbamate

Base Information

Chemical Name:Ethyl (2-oxo-2-phenylethyl)carbamate
CAS No.:59840-70-9
Molecular Formula:C11H13NO3
Molecular Weight:207.229
Hs Code.:
DSSTox Substance ID:DTXSID50497103
Wikidata:Q82346474

Synonyms:ethyl (2-oxo-2-phenylethyl)carbamate;59840-70-9;ethyl N-phenacylcarbamate;SCHEMBL10782158;DTXSID50497103;AKOS005438246;VS-00977;ETHYL N-(2-OXO-2-PHENYLETHYL)CARBAMATE

Suppliers and Price of Ethyl (2-oxo-2-phenylethyl)carbamate

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 1 raw suppliers

Chemical Property of Ethyl (2-oxo-2-phenylethyl)carbamate

Chemical Property:

PSA：58.89000
LogP:1.81980
XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:207.08954328
Heavy Atom Count:15
Complexity:222

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)NCC(=O)C1=CC=CC=C1

Technology Process of Ethyl (2-oxo-2-phenylethyl)carbamate

There total 5 articles about Ethyl (2-oxo-2-phenylethyl)carbamate 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:

: 13735-81-4
1-styrenyloxytrimethylsilane

: 817-87-8
ethyl azidocarbonate

: 59840-70-9
α-(ethoxycarbonylamino)acetophenone

: 582-24-1
1-phenyl-2-hydroxyethanone

Guidance literature:: With silica gel; Multistep reaction. Yields of byproduct given; 1.) 110 deg C, 15 h, 2.) CHCl₃, r.t., 20 h;
DOI:10.1016/S0040-4039(00)81473-2

Reference yield:

: 5468-37-1
2-aminoacetophenone hydrochloride

: 541-41-3
chloroformic acid ethyl ester

: 59840-70-9
α-(ethoxycarbonylamino)acetophenone

Guidance literature:: With pyridine; for 10h; Ambient temperature;
DOI:10.1246/bcsj.66.1216

Reference yield:

: 532-27-4,108321-66-0,164322-25-2
1-chloroacetophenone

: 59840-70-9
α-(ethoxycarbonylamino)acetophenone

Guidance literature:: Multi-step reaction with 2 steps

1: 20 °C / aus der additionellen Verbindung, durch Einw_. von alkoh. Salzsaeure

2: sodium bicarbonate; water

With water; sodium hydrogencarbonate;