2,6-Di(tert-butyl)-4-(2,4,6-trimethylbenzyl)phenol

Base Information

Chemical Name:2,6-Di(tert-butyl)-4-(2,4,6-trimethylbenzyl)phenol
CAS No.:59778-96-0
Molecular Formula:C₂₄H₃₄O
Molecular Weight:338.533
Hs Code.:
Mol file:59778-96-0.mol

Synonyms:3',5'-Di-tert.-butyl-4'-hydroxybenzylmesitylen;2,6-Ditert-butyl-4-(mesitylmethyl)phenol;Phenol,2,6-bis(1,1-dimethylethyl)-4-[(2,4,6-trimethylphenyl)methyl];2,6-Di-tert-butyl-4-(2,4,6-trimethylbenzyl)phenol;

Suppliers and Price of 2,6-Di(tert-butyl)-4-(2,4,6-trimethylbenzyl)phenol

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 4 raw suppliers

Chemical Property of 2,6-Di(tert-butyl)-4-(2,4,6-trimethylbenzyl)phenol

Chemical Property:

PSA：20.23000
LogP:6.50320

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2,6-Di(tert-butyl)-4-(2,4,6-trimethylbenzyl)phenol

There total 2 articles about 2,6-Di(tert-butyl)-4-(2,4,6-trimethylbenzyl)phenol 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: 36.0%

: 128-37-0
2,6-di-tert-butyl-4-methyl-phenol

: 2926-29-6
Langlois reagent

: 108-67-8
1,3,5-trimethyl-benzene

: 59778-96-0
2,6-di-tert-butyl-4-(2,4,6-trimethylbenzyl)phenol

: 3360-56-3
1,3,5-trimethyl-2-trifluoromethylbenzene

: 2,6-di-tert-butyl-4-(2,2,2-trifluoroethyl)phenol

Guidance literature:: With lithium perchlorate; 9-(2-mesityl)-10-methylacridinium perchlorate; In acetonitrile; at 23 ℃; for 16h; Inert atmosphere; Irradiation; Electrochemical reaction;
DOI:10.1002/chem.201905774