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5-Iodo-1,2,3-trimethylbenzene

Base Information
  • Chemical Name:5-Iodo-1,2,3-trimethylbenzene
  • CAS No.:41381-34-4
  • Molecular Formula:C9H11I
  • Molecular Weight:246.091
  • Hs Code.:
  • Mol file:41381-34-4.mol
5-Iodo-1,2,3-trimethylbenzene

Synonyms:5-Iodo-1,2,3-trimethylbenzene

Suppliers and Price of 5-Iodo-1,2,3-trimethylbenzene
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
  • Crysdot
  • 5-Iodo-1,2,3-trimethylbenzene 96%
  • 5g
  • $ 1078.00
  • Crysdot
  • 5-Iodo-1,2,3-trimethylbenzene 96%
  • 1g
  • $ 335.00
  • Ambeed
  • 5-Iodo-1,2,3-trimethylbenzene 96%
  • 250mg
  • $ 84.00
  • Ambeed
  • 5-Iodo-1,2,3-trimethylbenzene 96%
  • 100mg
  • $ 57.00
  • Ambeed
  • 5-Iodo-1,2,3-trimethylbenzene 96%
  • 1g
  • $ 208.00
  • Alichem
  • 5-Iodo-1,2,3-trimethylbenzene
  • 5g
  • $ 1098.88
  • Alichem
  • 5-Iodo-1,2,3-trimethylbenzene
  • 1g
  • $ 351.52
  • AK Scientific
  • 5-Iodo-1,2,3-trimethylbenzene
  • 100mg
  • $ 136.00
Total 6 raw suppliers
Chemical Property of 5-Iodo-1,2,3-trimethylbenzene
Chemical Property:
  • PSA:0.00000 
  • LogP:3.21640 
  • Storage Temp.:2-8°C(protect from light) 
Purity/Quality:

97% *data from raw suppliers

5-Iodo-1,2,3-trimethylbenzene 96% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 5-Iodo-1,2,3-trimethylbenzene

There total 1 articles about 5-Iodo-1,2,3-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:
Diazotization;
Guidance literature:
With 1-butyl-2,3-dimethylimidazolium tetrafluoroborate; C18H27Cl2N3OPd; triethylamine; triphenylphosphine; at 100 ℃; for 12h; regioselective reaction; Inert atmosphere; Schlenk technique;
DOI:10.1016/j.jorganchem.2015.05.020
Guidance literature:
With sulfuric acid; iodine; periodic acid; In acetic acid;
DOI:10.1246/bcsj.46.589
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