rel-(2R,4aS,6S,8aR)-Decahydro-2-(2-propen-1-yloxy)-6-(trans-4-propylcyclohexyl)naphthalene

Base Information

Chemical Name:rel-(2R,4aS,6S,8aR)-Decahydro-2-(2-propen-1-yloxy)-6-(trans-4-propylcyclohexyl)naphthalene
CAS No.:85603-97-0
Molecular Formula:C₂₂H₃₈O
Molecular Weight:318.543
Hs Code.:
DSSTox Substance ID:DTXSID801122065
Mol file:85603-97-0.mol

Synonyms:DTXSID801122065;rel-(2R,4aS,6S,8aR)-Decahydro-2-(2-propen-1-yloxy)-6-(trans-4-propylcyclohexyl)naphthalene;85603-97-0

Suppliers and Price of rel-(2R,4aS,6S,8aR)-Decahydro-2-(2-propen-1-yloxy)-6-(trans-4-propylcyclohexyl)naphthalene

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 3 raw suppliers

Chemical Property of rel-(2R,4aS,6S,8aR)-Decahydro-2-(2-propen-1-yloxy)-6-(trans-4-propylcyclohexyl)naphthalene

Chemical Property:

PSA：9.23000
LogP:6.38050
XLogP3:7.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:6
Exact Mass:318.292265831
Heavy Atom Count:23
Complexity:355

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC1CCC(CC1)C2CCC3CC(CCC3C2)OCC=C
Isomeric SMILES:CCCC1CCC(CC1)[C@@H]2CC[C@H]3C[C@H](CC[C@@H]3C2)OCC=C

Technology Process of rel-(2R,4aS,6S,8aR)-Decahydro-2-(2-propen-1-yloxy)-6-(trans-4-propylcyclohexyl)naphthalene

There total 3 articles about rel-(2R,4aS,6S,8aR)-Decahydro-2-(2-propen-1-yloxy)-6-(trans-4-propylcyclohexyl)naphthalene 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: 70.0%

: 85603-77-6
(2S,4aR,6R,8aS/2R,4aS,6S,8aR)-Decahydro-6-(trans-4-propylcyclohexyl)-2-naphthalinol

: 109-64-8
1,3-dibromo-propane

: 85603-97-0
(2S,4aR,6R,8aS)-2-Allyloxy-6-(4-propyl-cyclohexyl)-decahydro-naphthalene

Guidance literature:: With potassium hydride; In tetrahydrofuran; Heating;

Reference yield:

: 85603-76-5
(4aR,6R/4aS,6S)-4,4a,5,6,7,8-Hexahydro-6-(trans-4-propylcyclohexyl)-2(3H)-naphthalinon

: 85603-97-0
(2S,4aR,6R,8aS)-2-Allyloxy-6-(4-propyl-cyclohexyl)-decahydro-naphthalene

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / Li, liq. NH₃ / tetrahydrofuran

2: 70 percent / KH / tetrahydrofuran / Heating

With ammonia; lithium; potassium hydride; In tetrahydrofuran;

Reference yield:

: 85603-75-4,85647-80-9,98855-60-8
2-(3-Oxobutyl)-4-(trans-4-propylcyclohexyl)cyclohexanon

: 85603-97-0
(2S,4aR,6R,8aS)-2-Allyloxy-6-(4-propyl-cyclohexyl)-decahydro-naphthalene

Guidance literature:: Multi-step reaction with 3 steps

1: 79 percent / Na-OMe / methanol / 1.5 h / Heating

2: 95 percent / Li, liq. NH₃ / tetrahydrofuran

3: 70 percent / KH / tetrahydrofuran / Heating

With ammonia; sodium methylate; lithium; potassium hydride; In tetrahydrofuran; methanol;