Phenyl(3-phenyl-1,2-oxazol-4-yl)methanone

Base Information

Chemical Name:Phenyl(3-phenyl-1,2-oxazol-4-yl)methanone
CAS No.:19688-06-3
Molecular Formula:C16H11NO2
Molecular Weight:249.269
Hs Code.:
DSSTox Substance ID:DTXSID10507570
Nikkaji Number:J396.768I
Wikidata:Q82363857

Synonyms:19688-06-3;Phenyl(3-phenyl-1,2-oxazol-4-yl)methanone;SCHEMBL14948995;DTXSID10507570

Suppliers and Price of Phenyl(3-phenyl-1,2-oxazol-4-yl)methanone

Supply Marketing:

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

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Chemical Property of Phenyl(3-phenyl-1,2-oxazol-4-yl)methanone

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:249.078978594
Heavy Atom Count:19
Complexity:306

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NOC=C2C(=O)C3=CC=CC=C3

Technology Process of Phenyl(3-phenyl-1,2-oxazol-4-yl)methanone

There total 14 articles about Phenyl(3-phenyl-1,2-oxazol-4-yl)methanone 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: 99.0%

: 127703-94-0
3-Phenyl-4-benzoyl-isoxazolon-⁽⁵⁾

: 19688-06-3
3-phenyl-4-benzoylisoxazole

Guidance literature:: With manganese(IV) oxide; In benzene; for 1h; Heating;

Reference yield: 73.0%

: 932-90-1,622-31-1,140461-24-1,140461-25-2,622-32-2
syn-benzaldehyde oxime

: 1131-80-2,1201-93-0,31919-75-2
(E)-3-(N,N-dimethylamino)-1-phenyl-2-propen-1-one

: 19688-06-3
3-phenyl-4-benzoylisoxazole

Guidance literature:: With [hydroxy(tosyloxy)iodo]benzene; In dichloromethane; at 20 ℃; for 24h; regioselective reaction; Inert atmosphere;
DOI:10.1002/ejoc.201901258

Reference yield:

: 14397-33-2
3-phenyl-2-isoxazoline

: 19688-06-3
3-phenyl-4-benzoylisoxazole

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) lithium diisoprorylamide, hexamethylphosphoric triamide / 1.) THF, hexane, -78 deg C, 2h, 2.) -78 deg C, 2h

2: K₂Cr₂O₇, H₂SO₄ / diethyl ether / 1.25 h / 0 °C

3: 99 percent / active MnO₂ / benzene / 1 h / Heating

With N,N,N,N,N,N-hexamethylphosphoric triamide; potassium dichromate; manganese(IV) oxide; sulfuric acid; lithium diisopropyl amide; In diethyl ether; benzene;