1-Phenyl-3-(5-phenyl-1,2,4-oxadiazol-3-yl)-1H-indazole

Base Information

Chemical Name:1-Phenyl-3-(5-phenyl-1,2,4-oxadiazol-3-yl)-1H-indazole
CAS No.:96798-87-7
Molecular Formula:C₂₁H₁₄N₄O
Molecular Weight:338.368
Hs Code.:
DSSTox Substance ID:DTXSID90540107
Wikidata:Q82415990

Synonyms:96798-87-7;DTXSID90540107;1-Phenyl-3-(5-phenyl-1,2,4-oxadiazol-3-yl)-1H-indazole

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

Supply Marketing:

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

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

Chemical Property:

XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:338.11676108
Heavy Atom Count:26
Complexity:463

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=NN(C4=CC=CC=C43)C5=CC=CC=C5

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

There total 2 articles about 1-Phenyl-3-(5-phenyl-1,2,4-oxadiazol-3-yl)-1H-indazole 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: 60.0%

: 96799-22-3
Acetic acid phenyl-phenylazo-(5-phenyl-[1,2,4]oxadiazol-3-yl)-methyl ester

: 96798-87-7
1-Phenyl-3-(5-phenyl-1,2,4-oxadiazol-3-yl)indazole

Guidance literature:: With aluminium trichloride; In benzene; for 2h; Ambient temperature;

Reference yield:

: 59785-50-1,74675-58-4,74675-59-5
(E)-3-benzoyl-5-pgenyl-1,2,4-oxadiazole phenylhydrazone

: 96798-87-7
1-Phenyl-3-(5-phenyl-1,2,4-oxadiazol-3-yl)indazole

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / benzene / Ambient temperature

2: 60 percent / aluminium chloride / benzene / 2 h / Ambient temperature

With aluminium trichloride; In benzene;