Diazene, bis(2,4,6-trimethylphenyl)-, (1E)-

Base Information

Chemical Name:Diazene, bis(2,4,6-trimethylphenyl)-, (1E)-
CAS No.:20488-59-9
Molecular Formula:C18H22N2
Molecular Weight:266.386
Hs Code.:

Synonyms:azomesitylene;(E)-1,2-dimesityldiazene;Azomesitylen;2,2',4,4',6,6'-hexamethylazobenzene;Bis-(2,4,6-trimethyl-phenyl)-diazene;trans-azomesitylene;1,2-dimesityldiazene;

Suppliers and Price of Diazene, bis(2,4,6-trimethylphenyl)-, (1E)-

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 0 raw suppliers

Chemical Property of Diazene, bis(2,4,6-trimethylphenyl)-, (1E)-

Chemical Property:

PSA：24.72000
LogP:5.95240

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Diazene, bis(2,4,6-trimethylphenyl)-, (1E)-

There total 35 articles about Diazene, bis(2,4,6-trimethylphenyl)-, (1E)- 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: 96.0%

: 88-05-1
2,4,6-trimethylaniline

: 20488-59-9
anti-2,2',4,4',6,6'-Hexamethylazobenzene

Guidance literature:: With pyridine; In dichloromethane; at 110 ℃; for 0.5h; under 37503.8 Torr; chemoselective reaction; Flow reactor;
DOI:10.1016/j.jcat.2017.02.012

Reference yield: 95.0%

: 14213-00-4
2,4,6-trimethylaniline azide

: 5692-66-0,20488-59-9,20488-60-2
2,2',4,4',6,6'-hexamethylazobenzene

Guidance literature:: With Fe(OC^tBu₂Ph)₂(tetrahydrofuran)₂; In benzene-d6; for 24h; Time; Inert atmosphere;
DOI:10.1021/acs.organomet.5b00231