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Benzene, (4-methylpentyl)-

Base Information Edit
  • Chemical Name:Benzene, (4-methylpentyl)-
  • CAS No.:4215-86-5
  • Molecular Formula:C12H18
  • Molecular Weight:162.275
  • Hs Code.:2902909090
  • Mol file:4215-86-5.mol
Benzene, (4-methylpentyl)-

Synonyms:Benzene, (4-methylpentyl)-;4-methyl-1-phenylpentane;2-methyl-5-phenylpentane;i-hexylbenzene;1-Phenyl-4-methylpentane;isohexylbenzene;

Suppliers and Price of Benzene, (4-methylpentyl)-
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 2 raw suppliers
Chemical Property of Benzene, (4-methylpentyl)- Edit
Chemical Property:
  • Melting Point:-25.43°C (estimate) 
  • Refractive Index:1.4969 (estimate) 
  • Boiling Point:217°C 
  • PSA:0.00000 
  • Density:0.8568 
  • LogP:3.66530 
Purity/Quality:

99%min *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of Benzene, (4-methylpentyl)-

There total 38 articles about Benzene, (4-methylpentyl)- 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 palladium on activated charcoal; hydrogen; In ethyl acetate; for 3h; Inert atmosphere;
DOI:10.1021/ja5015508
Guidance literature:
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In benzene; for 2h; Heating;
DOI:10.1021/ja0462777
Guidance literature:
With C17H21CuN4O(1+)*CF3O3S(1-); lithium methanolate; In tetrahydrofuran; at 0 ℃; for 8h; Schlenk technique; Inert atmosphere;
DOI:10.1039/C8DT03210F
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