2,4-Diiodo-6-nitrophenol

Base Information

• Chemical Name: 2,4-Diiodo-6-nitrophenol
• CAS No.: 20294-48-8
• Molecular Formula: C6H3I2NO3
• Molecular Weight: 390.904
• DSSTox Substance ID: DTXSID60552035
• Nikkaji Number: J444.980K
• Wikidata: Q82432003

Synonyms:2,4-diiodo-6-nitrophenol;20294-48-8;SCHEMBL1530400;DTXSID60552035;NS00133744;G64728

Chemical Property of 2,4-Diiodo-6-nitrophenol

Chemical Property:

• XLogP3: 3.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 390.82024
• Heavy Atom Count: 12
• Complexity: 184

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(C=C(C(=C1[N+](=O)[O-])O)I)I

Technology Process of 2,4-Diiodo-6-nitrophenol

There total 21 articles about 2,4-Diiodo-6-nitrophenol 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%

2-hydroxynitrobenzene (88-75-5,78813-12-4) → diiodo-4,6 nitro-2 phenol (20294-48-8)

Guidance literature:

With sodium periodate; sulfuric acid; iodine; potassium iodide; sodium sulfite; In water; acetic acid; at 25 ℃; for 4h;

DOI:10.1134/S1070428016030234

Reference yield: 27.0%

p-Iodophenol (540-38-5) → 4-iodo-2-nitrophenol (21784-73-6) + 2-iodo-4-nitrophenol (89487-91-2) + diiodo-4,6 nitro-2 phenol (20294-48-8)

Guidance literature:

With ammonium cerium(IV) nitrate; In acetonitrile; at 20 ℃; for 2h;

DOI:10.1002/jccs.200500086

Reference yield: 25.0%

p-Iodophenol (540-38-5) → diiodo-4,6 nitro-2 phenol (20294-48-8)

Guidance literature:

With iodine; silver nitrate; In acetonitrile; for 2h; Ambient temperature;

upstream raw materials:

2,4-diiodophenol

2,4,6-Triiodophenol

3-nitrosalicylic acid

4-iodo-2-nitrophenol

Downstream raw materials:

2,4-diiodo-6-nitroanisole

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