1,2-Diiodo-4,5-di-n-butoxybenzene

Base Information

Chemical Name:1,2-Diiodo-4,5-di-n-butoxybenzene
CAS No.:1005340-01-1
Molecular Formula:C₁₄H₂₀I₂O₂
Molecular Weight:474.121
Hs Code.:
Mol file:1005340-01-1.mol

Synonyms:1,2-dibutoxy-4,5-diiodobenzene

Suppliers and Price of 1,2-Diiodo-4,5-di-n-butoxybenzene

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

Strem Chemicals
1,2-Diiodo-4,5-di-n-butoxybenzene
1g
$ 354.00

Strem Chemicals
1,2-Diiodo-4,5-di-n-butoxybenzene
250mg
$ 118.00

American Custom Chemicals Corporation
1,2-DIIODO-4,5-DI-N-BUTOXYBENZENE 95.00%
5MG
$ 502.73

Total 3 raw suppliers

Chemical Property of 1,2-Diiodo-4,5-di-n-butoxybenzene

Chemical Property:

Boiling Point:423.8±45.0 °C(Predicted)
Density:1.689±0.06 g/cm3(Predicted)

Purity/Quality:

97% ^*data from raw suppliers

1,2-Diiodo-4,5-di-n-butoxybenzene ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1,2-Diiodo-4,5-di-n-butoxybenzene

There total 2 articles about 1,2-Diiodo-4,5-di-n-butoxybenzene 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: 94.0%

: 20367-35-5
1,2-dibutoxybenzene

: 1005340-01-1
1,2-dibutoxy-4,5-diiodobenzene

Guidance literature:: With iodine; periodic acid; In ethanol; at 70 ℃;
DOI:10.1002/chem.201301262

Reference yield:

: 120-80-9,19481-10-8,37349-32-9
benzene-1,2-diol

: 1005340-01-1
1,2-dibutoxy-4,5-diiodobenzene

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile

2: iodine; iodic acid; sulfuric acid / acetic acid; tetrachloromethane

With sulfuric acid; iodine; iodic acid; potassium carbonate; In tetrachloromethane; acetic acid; acetonitrile;
DOI:10.1016/j.polymer.2013.09.017

Reference yield: 81.0%

: 860021-91-6
2-ethynyl-3-((triisopropylsilyl)ethynyl)pyridine

: 1005340-01-1
1,2-dibutoxy-4,5-diiodobenzene

: 1031223-84-3
C₅₀H₆₈N₂O₂Si₂

Guidance literature:: With diisopropylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; at 80 ℃; for 72h;
DOI:10.1021/jo7019724