1,1'-[3-(4-tert-Butoxyphenyl)cycloprop-1-ene-1,2-diyl]dibenzene

Base Information

Chemical Name:1,1'-[3-(4-tert-Butoxyphenyl)cycloprop-1-ene-1,2-diyl]dibenzene
CAS No.:89745-96-0
Molecular Formula:C₂₅H₂₄O
Molecular Weight:340.465
Hs Code.:
DSSTox Substance ID:DTXSID00529903

Synonyms:89745-96-0;DTXSID00529903;1,1'-[3-(4-tert-Butoxyphenyl)cycloprop-1-ene-1,2-diyl]dibenzene

Suppliers and Price of 1,1'-[3-(4-tert-Butoxyphenyl)cycloprop-1-ene-1,2-diyl]dibenzene

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 1,1'-[3-(4-tert-Butoxyphenyl)cycloprop-1-ene-1,2-diyl]dibenzene

Chemical Property:

XLogP3:5.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:340.182715385
Heavy Atom Count:26
Complexity:463

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC1=CC=C(C=C1)C2C(=C2C3=CC=CC=C3)C4=CC=CC=C4

Technology Process of 1,1'-[3-(4-tert-Butoxyphenyl)cycloprop-1-ene-1,2-diyl]dibenzene

There total 3 articles about 1,1'-[3-(4-tert-Butoxyphenyl)cycloprop-1-ene-1,2-diyl]dibenzene 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:

: 89745-94-8
1-(1,1-dimethylethoxy)-4-(2-phenylethenyl)benzene

: 89745-96-0
4-(diphenylcyclopropenyl)-t-butoxybenzene

Guidance literature:: Multi-step reaction with 2 steps

1: 67 percent / benzene / 1.5 h / Heating

2: potassium t-butoxide / tetrahydrofuran / 30 min at 0 deg C, then 15 min at room temperature

With potassium tert-butylate; In tetrahydrofuran; benzene;
DOI:10.1016/S0040-4039(01)91151-7

Reference yield:

: 4460-46-2
3-chloro-3-phenyl-3H-diazirine

: 89745-96-0
4-(diphenylcyclopropenyl)-t-butoxybenzene

Guidance literature:: Multi-step reaction with 2 steps

1: 67 percent / benzene / 1.5 h / Heating

2: potassium t-butoxide / tetrahydrofuran / 30 min at 0 deg C, then 15 min at room temperature

With potassium tert-butylate; In tetrahydrofuran; benzene;
DOI:10.1016/S0040-4039(01)91151-7

Reference yield:

: 89745-95-9
p-(2-chloro-2,3-diphenylcyclopropyl)-t-butoxybenzene

: 89745-96-0
4-(diphenylcyclopropenyl)-t-butoxybenzene

: 4-(diphenylcyclopropenyl)-t-butoxybenzene

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; Title compound not separated from byproducts; 30 min at 0 deg C, then 15 min at room temperature;
DOI:10.1016/S0040-4039(01)91151-7