1,4-Diphenyl-1,3-cycloheptadiene

Base Information

Chemical Name:1,4-Diphenyl-1,3-cycloheptadiene
CAS No.:94333-14-9
Molecular Formula:C₁₉H₁₈
Molecular Weight:246.352
Hs Code.:
DSSTox Substance ID:DTXSID60576519
Nikkaji Number:J1.302.643B

Synonyms:1,4-Diphenyl-1,3-cycloheptadiene;94333-14-9;DTXSID60576519;1,4-Diphenylcyclohepta-1,3-diene

Suppliers and Price of 1,4-Diphenyl-1,3-cycloheptadiene

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 1,4-Diphenyl-1,3-cycloheptadiene

Chemical Property:

XLogP3:5.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:2
Exact Mass:246.140850574
Heavy Atom Count:19
Complexity:301

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(=CC=C(C1)C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of 1,4-Diphenyl-1,3-cycloheptadiene

There total 6 articles about 1,4-Diphenyl-1,3-cycloheptadiene 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: 100.0%

: 95278-10-7
1,4-diphenylbicyclo<3.2.0>hept-2-ene

: 94333-14-9
1,4-diphenyl-1,3-cycloheptadiene

Guidance literature:: In benzene; Mechanism; Ambient temperature; Irradiation;
DOI:10.1246/cl.1992.803

Reference yield:

: 138153-10-3
2,6-Diphenyltricyclo<4.1.0.0^2,7>heptan

: 94333-14-9
1,4-diphenyl-1,3-cycloheptadiene

Guidance literature:: In benzene-d6; at 137 ℃; for 7h;

Reference yield:

: 21025-06-9
1,3-Diphenyl-1-cyclohexen

: 94333-14-9
1,4-diphenyl-1,3-cycloheptadiene

Guidance literature:: Multi-step reaction with 3 steps

1: 39 percent / 50percent NaOH, tri-n-butylamine / 1 h / 0 °C

2: 10 percent / CH₃Li / various solvent(s); diethyl ether / 0.67 h / 0 °C

3: benzene-d6 / 7 h / 137 °C

With sodium hydroxide; tributyl-amine; methyllithium; In diethyl ether; benzene-d6;