1,3,5-Tris(iodomethyl)benzene

Base Information

Chemical Name:1,3,5-Tris(iodomethyl)benzene
CAS No.:90678-60-7
Molecular Formula:C9H9I3
Molecular Weight:497.884
Hs Code.:
DSSTox Substance ID:DTXSID70514205
Nikkaji Number:J2.714.109I
Wikidata:Q82374386

Synonyms:1,3,5-tris(iodomethyl)benzene;90678-60-7;SCHEMBL5442950;DTXSID70514205

Suppliers and Price of 1,3,5-Tris(iodomethyl)benzene

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

Total 2 raw suppliers

Chemical Property of 1,3,5-Tris(iodomethyl)benzene

Chemical Property:

PSA：0.00000
LogP:4.49160
XLogP3:4.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:3
Exact Mass:497.7838
Heavy Atom Count:12
Complexity:91.2

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=C(C=C(C=C1CI)CI)CI

Technology Process of 1,3,5-Tris(iodomethyl)benzene

There total 3 articles about 1,3,5-Tris(iodomethyl)benzene 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: 87.0%

: 18226-42-1
1,3,5-Tris(bromomethyl)benzene

: 90678-60-7
1,3,5-tris(iodomethyl)benzene

Guidance literature:: With sodium iodide; In acetone; at 20 ℃; for 1h;
DOI:10.1002/chem.201406492

Reference yield:

: 4464-18-0
1,3,5-tris(hydroxymethyl)benzene

: 90678-60-7
1,3,5-tris(iodomethyl)benzene

Guidance literature:: With hydrogen iodide; In diethyl ether; Yield given; 1.) -30 deg C, 5 min; 2.) room temp., 0.5 h;
DOI:10.1055/s-1988-27748

Reference yield:

: 108-67-8
1,3,5-trimethyl-benzene

: 90678-60-7
1,3,5-tris(iodomethyl)benzene

Guidance literature:: Multi-step reaction with 2 steps

1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / benzene / 10 h / Reflux

2: sodium iodide / acetone / 1 h / 20 °C

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); sodium iodide; In acetone; benzene;
DOI:10.1002/chem.201406492