1-(4-(trans-4-n-heptylcyclohexyl)phenyl)-2-(4-trifluoromethylphenyl)ethene

Base Information

Chemical Name:1-(4-(trans-4-n-heptylcyclohexyl)phenyl)-2-(4-trifluoromethylphenyl)ethene
CAS No.:122161-22-2
Molecular Formula:C₂₈H₃₅F₃
Molecular Weight:428.581
Hs Code.:

Synonyms:1-(4-(trans-4-n-heptylcyclohexyl)phenyl)-2-(4-trifluoromethylphenyl)ethene

Suppliers and Price of 1-(4-(trans-4-n-heptylcyclohexyl)phenyl)-2-(4-trifluoromethylphenyl)ethene

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
Packaging
price

Total 0 raw suppliers

Chemical Property of 1-(4-(trans-4-n-heptylcyclohexyl)phenyl)-2-(4-trifluoromethylphenyl)ethene

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-(4-(trans-4-n-heptylcyclohexyl)phenyl)-2-(4-trifluoromethylphenyl)ethene

There total 5 articles about 1-(4-(trans-4-n-heptylcyclohexyl)phenyl)-2-(4-trifluoromethylphenyl)ethene 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:

: 61204-03-3
4-(trans-4-heptylcyclohexyl)benzonitrile

: 122161-22-2
1-(4-(trans-4-n-heptylcyclohexyl)phenyl)-2-(4-trifluoromethylphenyl)ethene

Guidance literature:: Multi-step reaction with 5 steps

1: sulfuric acid, water / 5 h / Heating

2: lithium aluminum hydride / tetrahydrofuran / Ambient temperature

3: 83 percent / 48 percent hydrobromic acid / 10 h / Heating

4: 100 percent / toluene / 6 h / Heating

5: 1.) butyllithium / 1.) hexan/ether, 2 h, room temperature, 2.) hexane/ether, 4 h, room temperature

With lithium aluminium tetrahydride; n-butyllithium; sulfuric acid; water; hydrogen bromide; In tetrahydrofuran; toluene;

Reference yield:

: 93205-75-5
4-(trans-4-n-heptylcyclohexyl)benzyl alcohol

: 122161-22-2
1-(4-(trans-4-n-heptylcyclohexyl)phenyl)-2-(4-trifluoromethylphenyl)ethene

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / 48 percent hydrobromic acid / 10 h / Heating

2: 100 percent / toluene / 6 h / Heating

3: 1.) butyllithium / 1.) hexan/ether, 2 h, room temperature, 2.) hexane/ether, 4 h, room temperature

With n-butyllithium; hydrogen bromide; In toluene;

Reference yield:

: 122161-21-1
4-(trans-4-n-heptylcyclohexyl)benzyl bromide

: 122161-22-2
1-(4-(trans-4-n-heptylcyclohexyl)phenyl)-2-(4-trifluoromethylphenyl)ethene

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / toluene / 6 h / Heating

2: 1.) butyllithium / 1.) hexan/ether, 2 h, room temperature, 2.) hexane/ether, 4 h, room temperature

With n-butyllithium; In toluene;