4-Amino-2,6-diiodophenol

Base Information

• Chemical Name: 4-Amino-2,6-diiodophenol
• CAS No.: 2297-82-7
• Molecular Formula: C6H5I2NO
• Molecular Weight: 360.921
• European Community (EC) Number: 898-058-2
• DSSTox Substance ID: DTXSID80501681
• Nikkaji Number: J2.609.398H
• Mol file: 2297-82-7.mol

Synonyms:4-Amino-2,6-diiodophenol;2297-82-7;Phenol, 4-amino-2,6-diiodo-;2,6-diiodo-4-aminophenol;SCHEMBL8439198;DTXSID80501681;CAA29782;AKOS034062742;EN300-395907;Z1416181930

Chemical Property of 4-Amino-2,6-diiodophenol

Chemical Property:

• XLogP3: 1.6
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 360.84606
• Heavy Atom Count: 10
• Complexity: 110

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(C=C(C(=C1I)O)I)N

Technology Process of 4-Amino-2,6-diiodophenol

There total 5 articles about 4-Amino-2,6-diiodophenol 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:

2,6-diiodo-4-nitrophenol (305-85-1) → 2,6-diiodo-4-aminophenol (2297-82-7)

Guidance literature:

With hydrogenchloride; tin(ll) chloride;

Reference yield:

4-nitro-phenol (100-02-7,78813-13-5,89830-32-0) → 2,6-diiodo-4-aminophenol (2297-82-7)

Guidance literature:

Multi-step reaction with 2 steps

1: aqueous acetic acid; ICl / 95 °C

2: tin; acetic acid

With tin; Iodine monochloride; acetic acid;

DOI:10.1577/1548-8659(2000)129<0194:GPSAOO>2.0.CO;2

Reference yield:

2,6-diiodo-4-phenylazo-phenol → 2,6-diiodo-4-aminophenol (2297-82-7)

Guidance literature:

With hydrogenchloride; acetic acid; tin(ll) chloride;

upstream raw materials:

2,6-diiodo-4-nitrophenol

4-nitro-phenol

Downstream raw materials:

iodine

2,6-diiodo-p-benzoquinone

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