2-Phenyl-1,3-oxazolidin-4-one

Base Information

Chemical Name:2-Phenyl-1,3-oxazolidin-4-one
CAS No.:38052-67-4
Molecular Formula:C9H9NO2
Molecular Weight:163.176
Hs Code.:
DSSTox Substance ID:DTXSID50496015
Mol file:38052-67-4.mol

Synonyms:2-phenyloxazolidin-4-one;38052-67-4;2-Phenyl-1,3-oxazolidin-4-one;SCHEMBL7710342;DTXSID50496015

Suppliers and Price of 2-Phenyl-1,3-oxazolidin-4-one

Supply Marketing:

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

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Chemical Property of 2-Phenyl-1,3-oxazolidin-4-one

Chemical Property:

XLogP3:0.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:163.063328530
Heavy Atom Count:12
Complexity:175

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(=O)NC(O1)C2=CC=CC=C2

Technology Process of 2-Phenyl-1,3-oxazolidin-4-one

There total 2 articles about 2-Phenyl-1,3-oxazolidin-4-one 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:

: 4461-33-0
benzoyl isocyanate

: 18107-18-1
diazomethyl-trimethyl-silane

: 38052-67-4
2-phenyl-1,3-oxazolidin-4-one

Guidance literature:: In diethyl ether; acetonitrile; at 20 ℃; for 0.75h;
DOI:10.1021/jo702305g

Reference yield:

: 1468-39-9
Isovaleric anhydride

: 38052-67-4
2-phenyl-1,3-oxazolidin-4-one

: 1402942-08-8
C₁₃H₁₅NO₃

: 1402942-54-4
2-phenyl-1,3-oxazolidin-4-one

: 38052-67-4
C₉H₉NO₂

Guidance literature:: 2-phenyl-1,3-oxazolidin-4-one; With (R)-(+)-2-phenyl-2,3-dihydrobenzo[d]imidazo[2,1-b]thiazole; N-ethyl-N,N-diisopropylamine; In chloroform; at 23 ℃; Resolution of racemate;

Isovaleric anhydride; With sodium sulfate; In chloroform; at 23 ℃; for 0.25h; enantioselective reaction; Resolution of racemate;
DOI:10.1021/ja306766n