2-(3-Ethenylphenyl)-5-phenyl-1,3,4-oxadiazole

Base Information

Chemical Name:2-(3-Ethenylphenyl)-5-phenyl-1,3,4-oxadiazole
CAS No.:308355-96-6
Molecular Formula:C₁₆H₁₂N₂O
Molecular Weight:248.284
Hs Code.:
DSSTox Substance ID:DTXSID00592415
Nikkaji Number:J1.630.286D
Wikidata:Q82486518
Mol file:308355-96-6.mol

Synonyms:2-(3-Ethenylphenyl)-5-phenyl-1,3,4-oxadiazole;308355-96-6;SCHEMBL6151722;DTXSID00592415

Suppliers and Price of 2-(3-Ethenylphenyl)-5-phenyl-1,3,4-oxadiazole

Supply Marketing:

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

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Chemical Property of 2-(3-Ethenylphenyl)-5-phenyl-1,3,4-oxadiazole

Chemical Property:

PSA：38.92000
LogP:4.04660
XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:248.094963011
Heavy Atom Count:19
Complexity:301

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CC1=CC(=CC=C1)C2=NN=C(O2)C3=CC=CC=C3

Technology Process of 2-(3-Ethenylphenyl)-5-phenyl-1,3,4-oxadiazole

There total 3 articles about 2-(3-Ethenylphenyl)-5-phenyl-1,3,4-oxadiazole 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: 54.0%

: 7486-35-3
tri-n-butyl(vinyl)tin

: 83817-44-1
2-(3-bromophenyl)-5-phenyl-1,3,4-oxadiazole

: 308355-96-6
2-(3-vinylphenyl)-5-phenyl-1,3,4-oxadiazole

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; In toluene; for 4h; Heating;
DOI:10.1039/b104674h

Reference yield:

: 18039-42-4,3999-10-8
5-Phenyl-1H-tetrazole

: 308355-96-6
2-(3-vinylphenyl)-5-phenyl-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / toluene / Heating

2: 54 percent / Pd(PPh₃)4 / toluene / 4 h / Heating

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; In toluene;
DOI:10.1039/b104674h

Reference yield:

: 1711-09-7
3-bromobenzoyl chloride

: 308355-96-6
2-(3-vinylphenyl)-5-phenyl-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / toluene / Heating

2: 54 percent / Pd(PPh₃)4 / toluene / 4 h / Heating

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; In toluene;
DOI:10.1039/b104674h