Phenol, 4-[1-(4-hydroxyphenyl)-1-methylethyl]-2-methyl-

Base Information

Chemical Name:Phenol, 4-[1-(4-hydroxyphenyl)-1-methylethyl]-2-methyl-
CAS No.:14151-63-4
Molecular Formula:C16H18O2
Molecular Weight:242.318
Hs Code.:
ChEMBL ID:CHEMBL2403345
DSSTox Substance ID:DTXSID70559717
Wikidata:Q82442542
Mol file:14151-63-4.mol

Synonyms:14151-63-4;Phenol, 4-[1-(4-hydroxyphenyl)-1-methylethyl]-2-methyl-;4-[2-(4-Hydroxyphenyl)propan-2-yl]-2-methylphenol;2-(4-hydroxy-3-methylphenyl)-2-(4'-hydroxyphenyl)propane;methylbisphenol-a;SCHEMBL1862016;CHEMBL2403345;DTXSID70559717;HFRAJYYHALXFLZ-UHFFFAOYSA-N;AKOS028114023;AS-69795;2-methyl-4,4'-(1-methylethylidene)bisphenol;D92891;2-(4-Hydroxy-3-methylphenyl)-2-(4-hydroxyphenyl)propane

Suppliers and Price of Phenol, 4-[1-(4-hydroxyphenyl)-1-methylethyl]-2-methyl-

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 3 raw suppliers

Chemical Property of Phenol, 4-[1-(4-hydroxyphenyl)-1-methylethyl]-2-methyl-

Chemical Property:

XLogP3:4.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:242.130679813
Heavy Atom Count:18
Complexity:266

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C=CC(=C1)C(C)(C)C2=CC=C(C=C2)O)O

Technology Process of Phenol, 4-[1-(4-hydroxyphenyl)-1-methylethyl]-2-methyl-

There total 7 articles about Phenol, 4-[1-(4-hydroxyphenyl)-1-methylethyl]-2-methyl- 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: 36.36%

: 80-05-7
BPA

: 616-38-6
carbonic acid dimethyl ester

: 6073-09-2
2,2-bis(4-hydroxyphenyl)propane monoacetate

: 10192-62-8
2,2-bis(4-acetoxyphenyl)propane

: 14151-63-4
2-(4-hydroxy-3-methylphenyl)-2-(4'-hydroxyphenyl)propane

: 19546-12-4
2-(4-hydroxy-3,5-dimethylphenyl)-2-(4'-hydroxyphenyl)propane

: 16530-58-8
p-<1-(4-methoxyphenyl)-1-methylethyl>phenol

Guidance literature:: With TiO₂#dotLi; In methanol; at 160 - 180 ℃; for 10h; Reagent/catalyst; Temperature; Inert atmosphere; Calcination;
DOI:10.1016/j.mcat.2018.12.022

Reference yield:

: 80-05-7
BPA

: 616-38-6
carbonic acid dimethyl ester

: 6073-09-2
2,2-bis(4-hydroxyphenyl)propane monoacetate

: 14151-63-4
2-(4-hydroxy-3-methylphenyl)-2-(4'-hydroxyphenyl)propane

: 19546-12-4
2-(4-hydroxy-3,5-dimethylphenyl)-2-(4'-hydroxyphenyl)propane

: 16530-58-8
p-<1-(4-methoxyphenyl)-1-methylethyl>phenol

Guidance literature:: With C₁₄H₈F₆OSn; at 165 ℃; for 10h; under 760.051 Torr; Reagent/catalyst; Temperature; Catalytic behavior; Inert atmosphere;
DOI:10.1007/s11696-019-00759-0

Reference yield:

: 99-76-3,156291-94-0
methyl 4-hydroxylbenzoate

: 14151-63-4
2-(4-hydroxy-3-methylphenyl)-2-(4'-hydroxyphenyl)propane

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / 0 - 20 °C

2: sulfuric acid / 0 - 20 °C

With sulfuric acid; In tetrahydrofuran;
DOI:10.1016/j.bmcl.2013.05.067