3-(Cyclohexyloxy)propan-1-ol

Base Information

• Chemical Name: 3-(Cyclohexyloxy)propan-1-ol
• CAS No.: 75322-09-7
• Molecular Formula: C9H18O2
• Molecular Weight: 158.241
• European Community (EC) Number: 854-181-3
• Mol file: 75322-09-7.mol

Synonyms:3-(cyclohexyloxy)propan-1-ol;75322-09-7;3-cyclohexyloxypropan-1-ol;3-cyclohexyloxypropyl alcohol;3-Cyclohexyloxy-propan-1-ol;SCHEMBL386704;3-(cyclohexoxy)-propan-1-ol;3-(cyclohexyloxy)-1-propanol;JZISPFMRVBHTCH-UHFFFAOYSA-N;AKOS009254416;CS-0247278;EN300-36269;A1-04662;F8881-1665;Z362785378

Chemical Property of 3-(Cyclohexyloxy)propan-1-ol

Chemical Property:

• PSA: 29.46000
• LogP: 1.71810
• XLogP3: 1.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 158.130679813
• Heavy Atom Count: 11
• Complexity: 87.6

Purity/Quality:

99% ^*data from raw suppliers

3-(cyclohexyloxy)propan-1-ol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCC(CC1)OCCCO
• Uses: 3-(cyclohexyloxy)propan-1-ol is a useful research chemical.

Technology Process of 3-(Cyclohexyloxy)propan-1-ol

There total 14 articles about 3-(Cyclohexyloxy)propan-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: 81.0%

3-(cyclohexyloxy)propionic acid (27912-81-8) → 3-cyclohexyloxypropyl alcohol (75322-09-7)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; for 48h; Ambient temperature;

Reference yield: 78.0%

cyclohexyl formate (4351-54-6) → 3-cyclohexyloxypropyl alcohol (75322-09-7)

Guidance literature:

With sodium tetrahydroborate; zirconium(IV) chloride; In tetrahydrofuran; at 20 ℃; for 0.333333h;

cyclohexyl formate; In tetrahydrofuran; at 20 ℃; for 24h;

Reference yield: 78.0%

cycloxexanone dimethyl ketal (933-40-4) + zirconium(IV) chloride (10026-11-6) → 3-cyclohexyloxypropyl alcohol (75322-09-7)

Guidance literature:

With hydrogenchloride; sodium borohydrid; In tetrahydrofuran;

upstream raw materials:

1,5-dioxa-spiro[5.5]undecane

sodium cyclohexanolate

1-chloro-3-hydroxypropane

cyclohexanol

Downstream raw materials:

3-(cyclohexyloxy)-1-propanol methanesulfonate (ester)

3-cyclohexyloxypropionaldehyde

(3-Vinyloxy-propoxy)-benzene

1-methoxy-3-phenoxy-propane