2-Cyclooctyl-2-propanol

Base Information

• Chemical Name: 2-Cyclooctyl-2-propanol
• CAS No.: 16624-06-9
• Molecular Formula: C₁₁H₂₂O
• Molecular Weight: 170.295
• Hs Code.: 2906199090
• DSSTox Substance ID: DTXSID50168083
• Nikkaji Number: J102.303I
• Wikidata: Q83037599
• Mol file: 16624-06-9.mol

Synonyms:2-cyclooctylpropan-2-ol;16624-06-9;2-CYCLOOCTYL-2-PROPANOL;alpha,alpha-Dimethylcyclooctanemethanol;Cyclooctanemethanol, .alpha.,.alpha.-dimethyl-;2-Cyclooctyl-2-propanol #;SCHEMBL9897847;DTXSID50168083;SSIKICQJPUCGEG-UHFFFAOYSA-N

Chemical Property of 2-Cyclooctyl-2-propanol

Chemical Property:

• Vapor Pressure: 0.00624mmHg at 25°C
• Boiling Point: 241.3°C at 760 mmHg
• Flash Point: 106.7°C
• PSA: 20.23000
• Density: 0.9g/cm³
• LogP: 3.11780
• XLogP3: 3.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 170.167065321
• Heavy Atom Count: 12
• Complexity: 121

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Other Classes -> Alcohols and Polyols, Other
• Canonical SMILES: CC(C)(C1CCCCCCC1)O

Technology Process of 2-Cyclooctyl-2-propanol

There total 2 articles about 2-Cyclooctyl-2-propanol 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:

methyl magnesium iodide (917-64-6) + 1-p-Toluolsulfonyloxymethyl-1-formyl-cycloheptan (24632-05-1) → 2-Cyclooctyl-propanol-(2) (16624-06-9)

Guidance literature:

In diethyl ether;

Reference yield:

cyclooctyl bromide (1556-09-8) + acetone (67-64-1) → 2-Cyclooctyl-propanol-(2) (16624-06-9)

Guidance literature:

Multistep reaction; (i) Mg, Et₂O, (ii) /BRN= 635680/;

upstream raw materials:

methyl magnesium iodide

1-p-Toluolsulfonyloxymethyl-1-formyl-cycloheptan

cyclooctyl bromide

acetone