Ethyl (2-oxo-2-phenylethoxy)carbamate

Base Information

Chemical Name:Ethyl (2-oxo-2-phenylethoxy)carbamate
CAS No.:88073-02-3
Molecular Formula:C₁₁H₁₃NO₄
Molecular Weight:223.229
Hs Code.:
DSSTox Substance ID:DTXSID00519405
Wikidata:Q82382561

Synonyms:88073-02-3;Ethyl (2-oxo-2-phenylethoxy)carbamate;DTXSID00519405

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

Supply Marketing:

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

Manufacturers and distributors:

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

Chemical Property:

Melting Point:81-82 °C
PSA：68.12000
Density:1.180±0.06 g/cm3(Predicted)
LogP:1.75140
XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:223.08445790
Heavy Atom Count:16
Complexity:236

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

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

There total 1 articles about Ethyl (2-oxo-2-phenylethoxy)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:

: 589-41-3
ethyl N-hydroxylcarbamate

: 70-11-1
α-bromoacetophenone

: 88073-02-3
ethyl phenacyloxycarbamate

Guidance literature:: With potassium hydroxide; Yield given. Multistep reaction; 1.) abs. ethanol, RT, 50 min; 2.) DMF, RT, 30 min;

Reference yield: 66.8%

: 88073-02-3
ethyl phenacyloxycarbamate

: 41260-63-3
ethyl (2-phenyl-1-hydroxy-2-oxoethyl)carbamate

Guidance literature:: With triethylamine; In benzene; for 1.5h; Ambient temperature;

Reference yield: 66.8%

: 88073-02-3
ethyl phenacyloxycarbamate

: 38192-19-7
methyl 2-phenyl-1-hydroxy-2-oxoethylcarbamate

: 41260-63-3
ethyl (2-phenyl-1-hydroxy-2-oxoethyl)carbamate

: 88073-11-4
methyl 2-p-bromophenyl-1-hydroxy-2-oxoethylcarbamate

: 88073-10-3
ethyl 2-p-bromophenyl-1-hydroxy-2-oxoethylcarbamate

Guidance literature:: With triethylamine; In benzene-d6; at 30 ℃; Rate constant; Mechanism; kinetic isotope effect; different reagents, solvent and reaction time;