4-Cyclohexylnaphthalen-1-ol

Base Information

Chemical Name:4-Cyclohexylnaphthalen-1-ol
CAS No.:64598-36-3
Molecular Formula:C₁₆H₁₈O
Molecular Weight:226.318
Hs Code.:
DSSTox Substance ID:DTXSID90558222
Wikidata:Q82440434

Synonyms:4-Cyclohexylnaphthalen-1-ol;64598-36-3;SCHEMBL11002147;DTXSID90558222

Suppliers and Price of 4-Cyclohexylnaphthalen-1-ol

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
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price

Total 1 raw suppliers

Chemical Property of 4-Cyclohexylnaphthalen-1-ol

Chemical Property:

XLogP3:5.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:226.135765193
Heavy Atom Count:17
Complexity:244

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC(CC1)C2=CC=C(C3=CC=CC=C23)O

Technology Process of 4-Cyclohexylnaphthalen-1-ol

There total 4 articles about 4-Cyclohexylnaphthalen-1-ol 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:

: 34224-97-0
1-Cyclohexyl-4-methoxynaphthalin

: 64598-36-3
4-Hydroxy-1-cyclohexyl-naphthalin

Guidance literature:: With boron tribromide; In dichloromethane; at -78 ℃;
DOI:10.1016/S0960-894X(02)00331-1

Reference yield:

: 2607-25-2
1-iodo-4-methoxynaphthalene

: 64598-36-3
4-Hydroxy-1-cyclohexyl-naphthalin

Guidance literature:: Multi-step reaction with 2 steps

1: Ni(dppp)Cl₂ / diethyl ether / Heating

2: BBr₃ / CH₂Cl₂ / -78 °C

With 1,3-bis[(diphenylphosphino)propane]dichloronickel(II); boron tribromide; In diethyl ether; dichloromethane;
DOI:10.1016/S0960-894X(02)00331-1