2,6-Diisopropyl-3-methylphenol

Base Information

Chemical Name:2,6-Diisopropyl-3-methylphenol
CAS No.:28434-93-7
Molecular Formula:C13H20 O
Molecular Weight:192.301
Hs Code.:2907199090
European Community (EC) Number:249-016-1
UNII:74I9X19WMR
DSSTox Substance ID:DTXSID20182635
Nikkaji Number:J79.311F
Wikidata:Q27266284
Metabolomics Workbench ID:44070
ChEMBL ID:CHEMBL27466
Mol file:28434-93-7.mol

Synonyms:2,6-Diisopropyl-3-methylphenol;2,6-Diisopropyl-m-cresol;28434-93-7;BRN 3247220;EINECS 249-016-1;Phenol, 2,6-diisopropyl-3-methyl-;3-methyl-2,6-di(propan-2-yl)phenol;UNII-74I9X19WMR;Phenol,3-methyl-2,6-bis(1-methylethyl)-;74I9X19WMR;CHEMBL27466;SCHEMBL1487336;2,6-Diisopropyl-m-cresol, 8CI;DTXSID20182635;2,6-Diisopropyl-3-methyl-phenol;CHEBI:172434;M-CRESOL, 2,6-DIISOPROPYL-;3-methyl-2,6-bis(propan-2-yl)phenol;3-METHYL-2,6-DIISOPROPYLPHENOL;LS-104414;Phenol, 3-methyl-2,6-bis(1-methylethyl)-;3-Methyl-2,6-bis(1-methylethyl)phenol, 9CI;Q27266284

Suppliers and Price of 2,6-Diisopropyl-3-methylphenol

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 7 raw suppliers

Chemical Property of 2,6-Diisopropyl-3-methylphenol

Chemical Property:

Vapor Pressure:0.0062mmHg at 25°C
Boiling Point:263.7°Cat760mmHg
Flash Point:118.5°C
PSA：20.23000
Density:0.941g/cm³
LogP:3.94740
XLogP3:4.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:192.151415257
Heavy Atom Count:14
Complexity:174

Purity/Quality:: 98%Min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 2,6-Diisopropyl-3-methylphenol

There total 5 articles about 2,6-Diisopropyl-3-methylphenol 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:

: 187737-37-7,13987-01-4,15220-87-8,9003-07-0,676-63-1,25085-53-4
propene

: 108-39-4
3-methyl-phenol

: 3228-02-2
3-Methyl-4-isopropylphenol

: 89-83-8
thymol

: 40625-96-5
5-methyl-2,4-diisopropylphenol

: 28434-93-7
3-methyl-2,6-diisopropylphenol

Guidance literature:: 1-butyl-3-methylimidazolium heptachlorodiindate (III); at 100 ℃; for 1.5h; Product distribution / selectivity; In ionic liquid;

Reference yield:

: 126570-35-2
2-Hydroxyisopropyl-3-methyl-6-isopropylphenol

: 28434-93-7
3-methyl-2,6-diisopropylphenol

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; acetic acid; Ambient temperature;

Reference yield:

: 6547-90-6
thymotic acid methyl ester

: 28434-93-7
3-methyl-2,6-diisopropylphenol

Guidance literature:: Multi-step reaction with 2 steps

1: 0.42 g / diethyl ether / 1) room temperature, 2) 1 h, reflux

2: 0.29 g / H₂ / Pd/C / ethanol; acetic acid / Ambient temperature

With hydrogen; palladium on activated charcoal; In diethyl ether; ethanol; acetic acid;