4-(Iodomethyl)benzaldehyde

Base Information

Chemical Name:4-(Iodomethyl)benzaldehyde
CAS No.:112812-08-5
Molecular Formula:C8H7IO
Molecular Weight:246.047
Hs Code.:
DSSTox Substance ID:DTXSID80552799
Wikidata:Q82433173

Synonyms:4-(Iodomethyl)benzaldehyde;112812-08-5;SCHEMBL10621952;DTXSID80552799

Suppliers and Price of 4-(Iodomethyl)benzaldehyde

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 4-(Iodomethyl)benzaldehyde

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:245.95416
Heavy Atom Count:10
Complexity:106

Purity/Quality:: ≥99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1CI)C=O

Technology Process of 4-(Iodomethyl)benzaldehyde

There total 5 articles about 4-(Iodomethyl)benzaldehyde 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: 98.0%

: 51359-78-5
4-(bromomethyl)benzaldehyde

: 112812-08-5
4-iodomethylbenzaldehyde

Guidance literature:: With sodium iodide; In acetonitrile; for 24h; Reflux;

Reference yield: 89.0%

: 1,4-bis-hydroxymethylbenzene+5% of terephthaldialdehyde

: 52010-97-6
4-(hydroxylmethyl)benzaldehyde

: 112812-08-5
4-iodomethylbenzaldehyde

Guidance literature:: With hydrogen iodide;

Reference yield:

: 100-39-0
benzyl bromide

: 112812-08-5
4-iodomethylbenzaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: titanium tetrachloride / dichloromethane / 1 h / 35 °C / Cooling with ice

2: sodium iodide / acetonitrile / 24 h / Reflux

With titanium tetrachloride; sodium iodide; In dichloromethane; acetonitrile;