1,3,5-TRIMETHYL-2-PROP-2-ENOXY-BENZENE

Base Information

Chemical Name:1,3,5-TRIMETHYL-2-PROP-2-ENOXY-BENZENE
CAS No.:5450-46-4
Molecular Formula:C12H16 O
Molecular Weight:176.258
Hs Code.:2909309090
Mol file:5450-46-4.mol

Synonyms:Benzene,1,3,5-trimethyl-2-(2-propenyloxy)- (9CI); Ether, allyl mesityl (6CI,8CI); Allyl2,4,6-trimethylphenyl ether; Allyl mesityl ether; NSC 7589

Suppliers and Price of 1,3,5-TRIMETHYL-2-PROP-2-ENOXY-BENZENE

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 5 raw suppliers

Chemical Property of 1,3,5-TRIMETHYL-2-PROP-2-ENOXY-BENZENE

Chemical Property:

Vapor Pressure:0.0341mmHg at 25°C
Boiling Point:250.6°Cat760mmHg
Flash Point:94.3°C
PSA：9.23000
Density:0.925g/cm³
LogP:3.17660

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1,3,5-TRIMETHYL-2-PROP-2-ENOXY-BENZENE

There total 12 articles about 1,3,5-TRIMETHYL-2-PROP-2-ENOXY-BENZENE 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: 95.0%

: 527-60-6
Mesitol

: 106-95-6
allyl bromide

: 5450-46-4
1,3,5-trimethyl-2-[(prop-2'-en-1'-yl)oxy]benzene

Guidance literature:: With potassium carbonate; In acetone; for 12h; Reflux;
DOI:10.1039/d1ob02227j

Reference yield: 85.0%

: allyl 2,4,6-trimethylphenyl carbonate

: 5450-46-4
1,3,5-trimethyl-2-[(prop-2'-en-1'-yl)oxy]benzene

Guidance literature:: With triphenylphosphine; tetrabutylammonium tricarbonylnitrosylferrate; In tert-butyl methyl ether; at 80 ℃; for 48h; regioselective reaction;
DOI:10.1021/ol902291z