N-(2-(5-Phenyl-1,2,4-oxadiazol-3-yl)phenyl)benzamide

Base Information

Chemical Name:N-(2-(5-Phenyl-1,2,4-oxadiazol-3-yl)phenyl)benzamide
CAS No.:29368-93-2
Molecular Formula:C21H15N3O2
Molecular Weight:341.369
Hs Code.:
DSSTox Substance ID:DTXSID10512785
Wikidata:Q82372183

Synonyms:29368-93-2;N-(2-(5-Phenyl-1,2,4-oxadiazol-3-yl)phenyl)benzamide;N-[2-(5-Phenyl-1,2,4-oxadiazol-3-yl)phenyl]benzamide;DTXSID10512785

Suppliers and Price of N-(2-(5-Phenyl-1,2,4-oxadiazol-3-yl)phenyl)benzamide

Supply Marketing:

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

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Chemical Property of N-(2-(5-Phenyl-1,2,4-oxadiazol-3-yl)phenyl)benzamide

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:341.116426730
Heavy Atom Count:26
Complexity:460

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NC(=NO2)C3=CC=CC=C3NC(=O)C4=CC=CC=C4

Technology Process of N-(2-(5-Phenyl-1,2,4-oxadiazol-3-yl)phenyl)benzamide

There total 4 articles about N-(2-(5-Phenyl-1,2,4-oxadiazol-3-yl)phenyl)benzamide 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: 92.0%

: 29083-89-4
3-(2-aminophenyl)-5-phenyl-1,2,4-oxadiazole

: 98-88-4
benzoyl chloride

: 29368-93-2
N-[2-(5-phenyl-[1,2,4]oxadiazol-3-yl)-phenyl]-benzamide

Guidance literature:: With triethylamine; In acetone;

Reference yield: 84.0%

: 29368-91-0
O-benzoyl-2-benzamidobenzamide oxime

: 29368-93-2
N-[2-(5-phenyl-[1,2,4]oxadiazol-3-yl)-phenyl]-benzamide

Guidance literature:: With sodium carbonate; In acetone; for 2h; Ambient temperature;

Reference yield:

: 93-89-0,99341-95-4
benzoic acid ethyl ester

: 29368-93-2
N-[2-(5-phenyl-[1,2,4]oxadiazol-3-yl)-phenyl]-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / sodium ethoxide / ethanol / 8 h / Heating

2: 92 percent / triethylamine / acetone

With sodium ethanolate; triethylamine; In ethanol; acetone;