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2-(3,5-Dimethylbenzyl)-1,3,5-trimethylbenzene

Base Information Edit
  • Chemical Name:2-(3,5-Dimethylbenzyl)-1,3,5-trimethylbenzene
  • CAS No.:729-65-7
  • Molecular Formula:C18H22
  • Molecular Weight:238.373
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20435875
  • Nikkaji Number:J390.812G
  • Wikidata:Q82250998
  • Mol file:729-65-7.mol
2-(3,5-Dimethylbenzyl)-1,3,5-trimethylbenzene

Synonyms:2-(3,5-dimethylbenzyl)-1,3,5-trimethylbenzene;STK331795;729-65-7;DTXSID20435875;LZNZMAZSWVVEBS-UHFFFAOYSA-N;2-(3,5-Dimethylbenzyl)mesitylene;AKOS005439438;1,3,5-trimethyl-2-(3',5'-dimethylbenzyl)benzene;1,3,5-trimethyl-2-(3', 5'-dimethylbenzyl)benzene

Suppliers and Price of 2-(3,5-Dimethylbenzyl)-1,3,5-trimethylbenzene
Supply Marketing:Edit
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 1 raw suppliers
Chemical Property of 2-(3,5-Dimethylbenzyl)-1,3,5-trimethylbenzene Edit
Chemical Property:
  • XLogP3:5.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:2
  • Exact Mass:238.172150702
  • Heavy Atom Count:18
  • Complexity:235
Purity/Quality:

95% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC(=CC(=C1)CC2=C(C=C(C=C2C)C)C)C
Technology Process of 2-(3,5-Dimethylbenzyl)-1,3,5-trimethylbenzene

There total 31 articles about 2-(3,5-Dimethylbenzyl)-1,3,5-trimethylbenzene 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:
Guidance literature:
With o-tetrachloroquinone; at 140 ℃; for 24h;
DOI:10.1081/SCC-120026326
Guidance literature:
With lithium trifluoroacetate; In trifluoroacetic acid; byproducts: CF3COOH; solns. of Tl(OCOCF3)3, arene, and CF3COOLi in degassed CF3COOH were mixed at 25°C under Ar in the dark, mixt. was stirred for a few min; rate consts. in the presence and in the absence of added CF3COOLi are given; solvent was removed in vacuo, residue identified by its (1)H NMR spectrum and via quant. converting into the corresponding iodide with KI followed by GC anal.; Kinetics;
DOI:10.1021/ja00335a039
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