2,4-Dichloro-6-iodophenol

Base Information

• Chemical Name: 2,4-Dichloro-6-iodophenol
• CAS No.: 2040-83-7
• Molecular Formula: C6H3Cl2IO
• Molecular Weight: 288.9
• Hs Code.: 2908199090
• European Community (EC) Number: 623-848-9
• DSSTox Substance ID: DTXSID80404249
• Nikkaji Number: J410.170G
• Wikidata: Q82208336
• Mol file: 2040-83-7.mol

Synonyms:2,4-dichloro-6-iodophenol;2040-83-7;Phenol, 2,4-dichloro-6-iodo-;2,4-Dichloro-6-iodo-phenol;SCHEMBL422660;DTXSID80404249;UMDKVOOEGYNMEB-UHFFFAOYSA-N;CAA04083;MFCD00086134;AKOS024332735;AB92899;BS-16517;CS-0157714;D83447

Chemical Property of 2,4-Dichloro-6-iodophenol

Chemical Property:

• PSA: 20.23000
• LogP: 3.30360
• Storage Temp.: 2-8°C(protect from light)
• XLogP3: 3.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 287.86057
• Heavy Atom Count: 10
• Complexity: 122

Purity/Quality:

95% ^*data from raw suppliers

2,4-Dichloro-6-iodophenol 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(C=C(C(=C1Cl)O)I)Cl

Technology Process of 2,4-Dichloro-6-iodophenol

There total 8 articles about 2,4-Dichloro-6-iodophenol 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:

4-chloro-2-iodo phenol (71643-66-8) → 2,4-dichloro-6-iodophenol (2040-83-7)

Guidance literature:

With tetrachloromethane; chlorine; at 0 ℃;

DOI:10.1039/jr9310000137

Reference yield:

3,5-dichlorosalicylic acid (320-72-9) → 2,4-dichloro-6-iodophenol (2040-83-7)

Guidance literature:

With sodium hydroxide; iodine; potassium iodide;

DOI:10.1557/JMR.2000.0135

Reference yield:

perchloric acid (7601-90-3) + sodium perchlorate + Iodine monochloride (7790-99-0) + 2,4-dichlorophenol (120-83-2,40477-79-0) → 2,4-dichloro-6-iodophenol (2040-83-7)

Guidance literature:

at 11 - 35 ℃; Kinetics;

DOI:10.1021/ja01537a027

upstream raw materials:

2-Iodophenol

3,5-dichlorosalicylic acid

4-chloro-2-iodo phenol

Iodine monochloride

Downstream raw materials:

3,5-dichloro-2-methoxyphenol

5,7-dichloro-2-methylbenzofuran

1,5-dichloro-3-iodo-2-methoxybenzene