2(3H)-Oxazolone, 5-(4-chlorophenyl)-

Base Information

Chemical Name:2(3H)-Oxazolone, 5-(4-chlorophenyl)-
CAS No.:61416-43-1
Molecular Formula:C₉H₆ClNO₂
Molecular Weight:195.605
Hs Code.:
DSSTox Substance ID:DTXSID10486811
Wikidata:Q82328289

Synonyms:2(3H)-Oxazolone, 5-(4-chlorophenyl)-;61416-43-1;DTXSID10486811

Suppliers and Price of 2(3H)-Oxazolone, 5-(4-chlorophenyl)-

Supply Marketing:

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

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Chemical Property of 2(3H)-Oxazolone, 5-(4-chlorophenyl)-

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:195.0087061
Heavy Atom Count:13
Complexity:244

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C2=CNC(=O)O2)Cl

Technology Process of 2(3H)-Oxazolone, 5-(4-chlorophenyl)-

There total 3 articles about 2(3H)-Oxazolone, 5-(4-chlorophenyl)- 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:

: 131554-52-4
3-[2-(4-chlorophenyl)-2-oxo-ethyl]thiazolidine-2,4-dione

: 61416-43-1
5-(4-chlorophenyl)-3H-oxazol-2-one

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; at 20 ℃;
DOI:10.1021/acs.jmedchem.0c01561

Reference yield:

: 536-38-9
4-chlorobenzoylmethyl bromide

: 61416-43-1
5-(4-chlorophenyl)-3H-oxazol-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 20 °C

2: lithium hydroxide / tetrahydrofuran / 20 °C

With potassium carbonate; lithium hydroxide; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/acs.jmedchem.0c01561