2-Oxazolidinone, 3-(1-oxo-3-phenyl-2-propenyl)-

Base Information

Chemical Name:2-Oxazolidinone, 3-(1-oxo-3-phenyl-2-propenyl)-
CAS No.:109853-54-5
Molecular Formula:C12H11NO3
Molecular Weight:217.224
Hs Code.:
DSSTox Substance ID:DTXSID70350362

Synonyms:109853-54-5;2-Oxazolidinone, 3-(1-oxo-3-phenyl-2-propenyl)-;cinnamoyl oxazolidinone;DTXSID70350362

Suppliers and Price of 2-Oxazolidinone, 3-(1-oxo-3-phenyl-2-propenyl)-

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 2-Oxazolidinone, 3-(1-oxo-3-phenyl-2-propenyl)-

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:217.07389321
Heavy Atom Count:16
Complexity:305

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COC(=O)N1C(=O)C=CC2=CC=CC=C2

Technology Process of 2-Oxazolidinone, 3-(1-oxo-3-phenyl-2-propenyl)-

There total 6 articles about 2-Oxazolidinone, 3-(1-oxo-3-phenyl-2-propenyl)- 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: 85.0%

: 497-25-6
dimethylenecyclourethane

: 621-82-9
Cinnamic acid

: 109853-54-5
N-cinnamoyl oxazolidin-2-one

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In dichloromethane; at 20 ℃; for 3.5h;
DOI:10.1055/s-2003-42117

Reference yield: 76.0%

: 497-25-6
dimethylenecyclourethane

: 102-92-1,17082-09-6
cinnamoyl chloride

: 109853-54-5
N-cinnamoyl oxazolidin-2-one

Guidance literature:: dimethylenecyclourethane; With n-butyllithium; In tetrahydrofuran; at 0 ℃; for 0.25h; Schlenk technique;

cinnamoyl chloride; In tetrahydrofuran; at 0 - 20 ℃; for 0.75h; Schlenk technique;
DOI:10.1021/acs.joc.8b01798