N-Benzyl-5-phenyl-1,3,4-oxadiazole-2-carbothioamide

Base Information

Chemical Name:N-Benzyl-5-phenyl-1,3,4-oxadiazole-2-carbothioamide
CAS No.:89515-46-8
Molecular Formula:C₁₆H₁₃N₃OS
Molecular Weight:295.365
Hs Code.:
DSSTox Substance ID:DTXSID70529192
Wikidata:Q82399425

Synonyms:89515-46-8;N-Benzyl-5-phenyl-1,3,4-oxadiazole-2-carbothioamide;DTXSID70529192

Suppliers and Price of N-Benzyl-5-phenyl-1,3,4-oxadiazole-2-carbothioamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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Total 0 raw suppliers

Chemical Property of N-Benzyl-5-phenyl-1,3,4-oxadiazole-2-carbothioamide

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:295.07793322
Heavy Atom Count:21
Complexity:340

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNC(=S)C2=NN=C(O2)C3=CC=CC=C3

Technology Process of N-Benzyl-5-phenyl-1,3,4-oxadiazole-2-carbothioamide

There total 2 articles about N-Benzyl-5-phenyl-1,3,4-oxadiazole-2-carbothioamide 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: 45.0%

: 89515-39-9
5-Phenyl-[1,3,4]oxadiazole-2-carbodithioic acid methyl ester

: 100-46-9
benzylamine

: 89515-46-8
5-Phenyl-[1,3,4]oxadiazole-2-carbothioic acid benzylamide

Guidance literature:: In ethanol; for 0.05h; Heating;

Reference yield:

: 33575-83-6
2-(chloromethyl)-5-phenyl-1,3,4-oxadiazole

: 89515-46-8
5-Phenyl-[1,3,4]oxadiazole-2-carbothioic acid benzylamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) S₈, NEt₃ / 1.) DMF, 2 h, 2.) 10 deg C

2: 45 percent / ethanol / 0.05 h / Heating

With sulfur; triethylamine; In ethanol;