4-Hydroxy-3-iodo-5-methoxybenzonitrile

Base Information

Chemical Name:4-Hydroxy-3-iodo-5-methoxybenzonitrile
CAS No.:834907-45-8
Molecular Formula:C₈H₆INO₂
Molecular Weight:275.046
Hs Code.:2926909090
DSSTox Substance ID:DTXSID30598864
Wikidata:Q82494669
Mol file:834907-45-8.mol

Synonyms:4-hydroxy-3-iodo-5-methoxybenzonitrile;834907-45-8;Benzonitrile, 4-hydroxy-3-iodo-5-methoxy-;4-Hydroxy-3-iodo-5-methoxy-benzonitrile;DTXSID30598864;MFCD01123028;STK348816;AKOS000304407;LS-12210;DB-075939;CS-0240344;EN300-227937

Suppliers and Price of 4-Hydroxy-3-iodo-5-methoxybenzonitrile

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 5 raw suppliers

Chemical Property of 4-Hydroxy-3-iodo-5-methoxybenzonitrile

Chemical Property:

PSA：53.25000
LogP:1.87708
XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:274.94433
Heavy Atom Count:12
Complexity:201

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C(=CC(=C1)C#N)I)O

Technology Process of 4-Hydroxy-3-iodo-5-methoxybenzonitrile

There total 1 articles about 4-Hydroxy-3-iodo-5-methoxybenzonitrile 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: 78.0%

: 4421-08-3
3-methoxy-4-hydroxybenzonitrile

: 834907-45-8
C₈H₆INO₂

Guidance literature:: With 2,2'-azinobis(3-ethylbenzthiazolinesulfonate); laccase; potassium iodide; In dimethyl sulfoxide; at 20 ℃; for 24h; pH=5; Enzymatic reaction;
DOI:10.1039/c9ra02541c