2,4-Dichloro-1-(4-iodo-3-methoxyphenoxy)benzene

Base Information

• Chemical Name: 2,4-Dichloro-1-(4-iodo-3-methoxyphenoxy)benzene
• CAS No.: 68534-30-5
• Molecular Formula: C₁₃H₉Cl₂IO₂
• Molecular Weight: 395.024
• DSSTox Substance ID: DTXSID50511111
• Wikidata: Q82369731

Synonyms:2,4-Dichloro-1-(4-iodo-3-methoxyphenoxy)benzene;68534-30-5;SCHEMBL11191505;DTXSID50511111

Chemical Property of 2,4-Dichloro-1-(4-iodo-3-methoxyphenoxy)benzene

Chemical Property:

• XLogP3: 5.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 393.90243
• Heavy Atom Count: 18
• Complexity: 267

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=C(C=CC(=C1)OC2=C(C=C(C=C2)Cl)Cl)I

Technology Process of 2,4-Dichloro-1-(4-iodo-3-methoxyphenoxy)benzene

There total 1 articles about 2,4-Dichloro-1-(4-iodo-3-methoxyphenoxy)benzene 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:

aminochlomethoxyfen (59683-60-2) → 2,4-Dichlor-3'-methoxy-4'-joddiphenylether (68534-30-5)

Guidance literature:

Multistep reaction; (i) aq. H₂SO₄, (ii) (diazotization), (iii) KI;

Reference yield:

Methyl 2-bromopropionate (5445-17-0) + 2,4-Dichlor-3'-methoxy-4'-joddiphenylether (68534-30-5) + copper(I) cyanide (544-92-3) → Methyl α-[2-cyano-5-(2,4-dichlorophenoxy)phenoxy]propionate (68533-46-0)

Guidance literature:

Multistep reaction; (i)/BRN= 3587244/, 1-methyl-pyrrolidin-2-one, (ii) aq. HI, Ac₂O, AcOH, (iii) /BRN= 1720592/, K₂CO₃;

upstream raw materials:

aminochlomethoxyfen

Downstream raw materials:

Methyl α-[2-cyano-5-(2,4-dichlorophenoxy)phenoxy]propionate

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