alpha-(1,1-Dimethylethyl)-2,4,6-trimethylbenzenemethanol

Base Information

• Chemical Name: alpha-(1,1-Dimethylethyl)-2,4,6-trimethylbenzenemethanol
• CAS No.: 66390-58-7
• Molecular Formula: C14H22O
• Molecular Weight: 206.328
• DSSTox Substance ID: DTXSID401216901

Synonyms:alpha-(1,1-Dimethylethyl)-2,4,6-trimethylbenzenemethanol;DTXSID401216901;66390-58-7

Chemical Property of alpha-(1,1-Dimethylethyl)-2,4,6-trimethylbenzenemethanol

Chemical Property:

• XLogP3: 3.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 206.167065321
• Heavy Atom Count: 15
• Complexity: 192

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC(=C(C(=C1)C)C(C(C)(C)C)O)C

Technology Process of alpha-(1,1-Dimethylethyl)-2,4,6-trimethylbenzenemethanol

There total 4 articles about alpha-(1,1-Dimethylethyl)-2,4,6-trimethylbenzenemethanol 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:

2,2-dimethyl-1-(2,4,6-trimethylphenyl)propan-1-one (2700-84-7) → 2,2-Dimethyl-1-(2,4,6-trimethyphenyl)-1-propanol (66390-58-7)

Guidance literature:

With ethanol; sodium;

Reference yield:

pivaloyl chloride (3282-30-2) → 2,2-Dimethyl-1-(2,4,6-trimethyphenyl)-1-propanol (66390-58-7)

Guidance literature:

Multi-step reaction with 2 steps

1: diethyl ether

2: sodium; ethanol

With diethyl ether; ethanol; sodium;

Reference yield:

2-mesitylmagnesium bromide (2633-66-1) → 2,2-Dimethyl-1-(2,4,6-trimethyphenyl)-1-propanol (66390-58-7)

Guidance literature:

Multi-step reaction with 2 steps

1: diethyl ether

2: sodium; ethanol

With diethyl ether; ethanol; sodium;

upstream raw materials:

2,2-dimethyl-1-(2,4,6-trimethylphenyl)propan-1-one

pivaloyl chloride

2-mesitylmagnesium bromide

Downstream raw materials:

2,2-dimethyl-1-(2,4,6-trimethylphenyl)propan-1-one

1-(2,2-Dimethylpropyl)-2,4,6-trimethylbenzol

Essigsaeure-2,2-dimethyl-1-(2,4,6-trimethylphenyl)propylester

meso-2,2,5,5-Tetramethyl-3,4-bis(2,4,6-trimethylphenyl)hexan

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