2-(Benzyloxy)cyclohexanol

Base Information

Chemical Name:2-(Benzyloxy)cyclohexanol
CAS No.:51329-29-4
Molecular Formula:C₁₃H₁₈O₂
Molecular Weight:206.285
Hs Code.:
European Community (EC) Number:872-145-5
Nikkaji Number:J2.092.826C
Mol file:51329-29-4.mol

Synonyms:2-(BENZYLOXY)CYCLOHEXAN-1-OL;408523-57-9;2-(Benzyloxy)cyclohexanol;rac trans-2-Benzyloxy-cyclohexanol;rac-(1R,2R)-2-(Benzyloxy)cyclohexan-1-ol;SCHEMBL18629949;BCA32929;MFCD29045640;AKOS011042983;EN300-718179

Suppliers and Price of 2-(Benzyloxy)cyclohexanol

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 2-(Benzyloxy)cyclohexanol

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:206.130679813
Heavy Atom Count:15
Complexity:175

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC(C(C1)O)OCC2=CC=CC=C2

Technology Process of 2-(Benzyloxy)cyclohexanol

There total 9 articles about 2-(Benzyloxy)cyclohexanol 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: 99.0%

: 1792-81-0
cis-1,2-cyclohexane

: 100-39-0
benzyl bromide

: 51329-29-4,51329-30-7,85761-38-2,85761-39-3,116661-88-2,116661-89-3,125992-58-7
(+/-)-cis-2-(benzyloxy)cyclohexanol

Guidance literature:: With 4-fluoroboronic acid; tetraethylammonium bromide; potassium carbonate; In acetonitrile; at 20 ℃; for 38h;
DOI:10.1016/j.tetlet.2009.01.063

Reference yield: 0.055%

: 84029-20-9,84049-34-3,103001-68-9,103001-69-0,148969-20-4
racemic cis-1-benzyloxy-7-oxabicyclo[4.1.0]heptane

: 51329-29-4,51329-30-7,85761-38-2,85761-39-3,116661-88-2,116661-89-3,125992-58-7
(+/-)-cis-2-(benzyloxy)cyclohexanol

: 114737-99-4
cis-3-benzyloxy-1-cyclohexanol

Guidance literature:: With lithium aluminium tetrahydride; (1,4,7,10-tetraoxacyclododecane); In pentane; for 5h; Yield given. Yields of byproduct given; Ambient temperature;
DOI:10.1016/S0040-4020(01)81219-9

Reference yield:

: 32700-48-4
[(cyclohex-2-en-1-yloxy)methyl]benzene

: 85761-38-2
(+/-)-trans-2-benzyloxycyclohexan-1-ol

: 51329-29-4,51329-30-7,85761-38-2,85761-39-3,116661-88-2,116661-89-3,125992-58-7
(+/-)-cis-2-(benzyloxy)cyclohexanol

: 114737-99-4
cis-3-benzyloxy-1-cyclohexanol

: 114738-00-0
trans-3-(benzyloxy)cyclohexanol

Guidance literature:: With sodium hydroperoxide; benzo[1,3,2]dioxaborole; Wilkinson's catalyst; at 25 ℃; Product distribution; without catalyst, other reagent for hydroboration;
DOI:10.1021/ja00228a068