729-65-7

Basic information

• Product Name: Benzene, 2-[(3,5-dimethylphenyl)methyl]-1,3,5-trimethyl-
• CAS NO: 729-65-7
• Molecular Formula: C18H22
• Molecular Weight: 238.373
• Mol File: 729-65-7.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: Benzene, 2-[(3,5-dimethylphenyl)methyl]-1,3,5-trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 2-[(3,5-dimethylphenyl)methyl]-1,3,5-trimethyl-(729-65-7)
• EPA Substance Registry System: Benzene, 2-[(3,5-dimethylphenyl)methyl]-1,3,5-trimethyl-(729-65-7)

Safety Data

• Hazardous Substances Data: 729-65-7(Hazardous Substances Data)

Upstream product

• 16340-64-0 (3.5-Dimethyl-phenyl)-(2.4.6-trimethyl-phenyl)-carbinol 
• 30930-49-5 bis(2-thiophenecarbonyl) peroxide 
• 108-67-8 1,3,5-trimethyl-benzene 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 27129-86-8 1-bromomethyl-3,5-dimethylbenzene 
• 90-44-8 anthracen-9(10H)-one 
• 21918-35-4 1,3-bis(3,5-dimethylphenyl)-2-propanone 
• 94-36-0 dibenzoyl peroxide 
• 7664-93-9 sulfuric acid 
• 64-19-7 acetic acid 
• 576-83-0 2,4,6-trimethylphenyl bromide 
• 10034-85-2 hydrogen iodide 
• 5779-95-3 3,5-dimethylbenzaldehyde 
• 24994-60-3 1-amino-1,2,4-triazole 

Downstream Products

• 16340-64-0 (3.5-Dimethyl-phenyl)-(2.4.6-trimethyl-phenyl)-carbinol 

Relevant articles and documents

Strategy for Selective Csp2-F and Csp2-Csp2Formations from Organoplatinum Complexes

By changing the parameters of fluorination reaction of bisaryl-platinum(II) complexes, each possible competitive pathway of Ar-Ar and Ar-F formation can be selectively controlled. It was discovered that steric hindrance, type of fluorinating reagent, and

A Simple Preparation of Diarylmethanes by Oxidative Friedel-Crafts Reaction of Methyl-Substituted Benzenes with o-Chloranil

The reaction of o-chloranil with some methyl-substituted benzenes at elevated temperature was found to be a simple and selective route toward diarylmethanes without need for prior preparation of benzyl halides.

The 1,2,4-triazolyl cation: Thermolytic and photolytic studies

The generation of the 1,2,4-triazolyl cation (1) has been attempted by the thermolysis and photolysis of 1-(1,2,4-triazol-4-yl)-2,4,6-trimethylpyridinium tetrafluoroborate (2) and the thermolysis of 1- and 4-diazonium-1,2,4-triazoles, using mainly mesitylene as the trapping agent. Thermolysis of 2 gave mostly 1,2,4-triazole, together with 3-(1,2,4-triazol-4-yl)-2,4,6-trimethylpyridine, 4-(1,2,4-triazol-4-ylmethyl)-2,6-dimethylpyridine, and 4-(2,4,6-trimethylbenzyl)-2,6-dimethylpyridine. Thermolysis, of each of the diazonium salts in the presence of mesitylene again gave mainly triazole together with very low yields of 1-(1,2,4-triazol-1-yl)-2,4,6-trimethylbenzene and the corresponding -4-yl isomer in about the same ratio. On the other hand, photolysis of 2 in mesitylene gave mainly 1-(1,2,4-triazol-1-yl)-2,4,6-trimethylbenzene. A photoinduced electron transfer from mesitylene to 2 has been observed and preliminary laser flash photolyses of 2 and the corresponding 2,4,6-triphenylpyridinium salt have been carried out. The observed transients are explained as arising from the first excited states of the pyridinium salts rather than from 1. Ab initio MO calculations are reported and indicate that the predicted electronic ground-state of the triazolyl cation is a triplet state of B1 symmetry with five π electrons, which corresponds to a diradical cation (1c). Possible mechanisms for the formation of the various products are proposed.