Cyclohexanol, 2-phenoxy-

Base Information

• Chemical Name: Cyclohexanol, 2-phenoxy-
• CAS No.: 100256-51-7
• Molecular Formula: C12H16O2
• Molecular Weight: 192.258
• DSSTox Substance ID: DTXSID10458694
• Nikkaji Number: J2.195.052A
• Mol file: 100256-51-7.mol

Synonyms:Cyclohexanol, 2-phenoxy-;2-phenoxycyclohexanol;100256-51-7;2-phenoxycyclohexan-1-ol;2-phenoxy-cyclohexanol;SCHEMBL1496724;DTXSID10458694;YQVLZECCVJWFMV-UHFFFAOYSA-N

Chemical Property of Cyclohexanol, 2-phenoxy-

Chemical Property:

• XLogP3: 2.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 192.115029749
• Heavy Atom Count: 14
• Complexity: 164

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCC(C(C1)O)OC2=CC=CC=C2

Technology Process of Cyclohexanol, 2-phenoxy-

There total 5 articles about Cyclohexanol, 2-phenoxy- 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: 92.0%

cyclohexene oxide (286-20-4) + sodium phenoxide (139-02-6) → 2-hydroxycyclohexyl phenyl ether (100256-51-7)

Guidance literature:

With cerium(IV) triflate; sodium dodecyl-sulfate; at 20 ℃; for 3h;

DOI:10.1081/SCC-120005998

Reference yield: 90.0%

cyclohexane-1,2-epoxide (286-20-4) + phenol (108-95-2,27073-41-2) → 2-hydroxycyclohexyl phenyl ether (100256-51-7)

Guidance literature:

With tetra-(n-butyl)ammonium iodide; at 80 ℃; for 70h;

Reference yield: 75.0%

4-nitro-phenol (100-02-7,78813-13-5,89830-32-0) + cyclohexane-1,2-epoxide (286-20-4) + phenol (108-95-2,27073-41-2) → 2-hydroxycyclohexyl phenyl ether (100256-51-7)

Guidance literature:

bismuth(lll) trifluoromethanesulfonate; In dichloromethane; at 20 ℃; for 2h;

DOI:10.1246/cl.2005.1142

upstream raw materials:

cyclohexene oxide

sodium phenoxide

cyclohexene

phenol

Downstream raw materials:

2-phenoxycyclohexanone

2-(4-tert-butylphenoxy)cyclohexanol