3,5-dimethylphenol

Base Information

• Chemical Name: 3,5-dimethylphenol
• CAS No.: 50356-23-5
• Molecular Formula: C₈H₁₀O
• Molecular Weight: 122.167
• Mol file: 50356-23-5.mol

Synonyms:C9H12

Chemical Property of 3,5-dimethylphenol

Chemical Property:

• Melting Point: 64oC
• Boiling Point: 219.5oC
• PSA: 0.00000
• LogP: 2.61180

Purity/Quality:

99%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 3,5-dimethylphenol

There total 52 articles about 3,5-dimethylphenol 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: 20.3%

m-xylene (108-38-3,104809-90-7) → 2.6-dimethylphenol (576-26-1,25134-01-4) + 1-Methyl-3-ethylbenzene (620-14-4) + 1,2-di-m-tolylethane (4662-96-8) + 3-methylbenzyl alcohol (587-03-1) + 2,4-Xylenol (105-67-9) + 3,5-Dimethylphenol (108-68-9,50356-23-5)

Guidance literature:

With peracetic acid; at 20 - 22 ℃; Product distribution; Irradiation; λ=2537 Angstroem;

DOI:10.1021/jo01293a004

Reference yield:

N,N,N',N'-Tetramethyl-acridine-3,6-diamine; compound with 3,5-dimethyl-phenol → acridine orange (494-38-2) + 3,5-Dimethylphenol (108-68-9,50356-23-5)

Guidance literature:

In benzonitrile; at 25 ℃; Equilibrium constant; ionic strength 0.1 M;

Reference yield:

N,N,N',N'-Tetramethyl-acridine-3,6-diamine; compound with 3,5-dimethyl-phenol → acridine orange (494-38-2) + 3,5-Dimethylphenol (108-68-9,50356-23-5)

Guidance literature:

In benzonitrile; at 25 ℃; Equilibrium constant; ionic strength 0.1 M;

upstream raw materials:

ortho-cresol

methanol

3,4-dimethyl-4-trichloromethyl-2,5-cyclohexadien-1-one

3,5-dimethyl-2-cyclohexen-1-one

Downstream raw materials:

3,5-Dimethyl-4-piperonyl-phenol

2-hydroxy-4,6-dimethylbenzaldehyde

3,5,3',5'-tetramethyl-2,2'-(2-aza-propanediyl)-di-phenol

5-acetoxy-m-xylene

Refernces

• 1、 -. "Method for hydrolyzing diarylether compound to generate aryl phenol compound". Paragraph 0135-0138. . Retrieved 2021/09/29.
• 2、 Moores, Lee C.,Kaur, Devinder,Smith, Mathew D.,Poole, James S.. "Regioselectivity of Hydroxyl Radical Reactions with Arenes in Nonaqueous Solutions". . p. 3260 - 3269. Retrieved 2019/03/11.