1-Chloro-4-(iodomethoxy)benzene

Base Information

• Chemical Name: 1-Chloro-4-(iodomethoxy)benzene
• CAS No.: 106261-89-6
• Molecular Formula: C7H6ClIO
• Molecular Weight: 268.482
• DSSTox Substance ID: DTXSID60545624
• Wikidata: Q82423181

Synonyms:1-Chloro-4-(iodomethoxy)benzene;106261-89-6;SCHEMBL4618802;DTXSID60545624

Chemical Property of 1-Chloro-4-(iodomethoxy)benzene

Chemical Property:

• XLogP3: 3.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 267.91519
• Heavy Atom Count: 10
• Complexity: 91.6

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC=C1OCI)Cl

Technology Process of 1-Chloro-4-(iodomethoxy)benzene

There total 1 articles about 1-Chloro-4-(iodomethoxy)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:

4-chloromethoxybenzene (623-12-1) → 4-chloro-α-iodoanisole (106261-89-6)

Guidance literature:

Multi-step reaction with 2 steps

1: Cl₂

2: 40 percent / NaI

With chlorine; sodium iodide;

DOI:10.1039/P19860000795

Reference yield: 46.0%

ethenesulfonic acid (1,1,3,3-tetramethyl-butyl)-amide (916247-28-4) + 4-chloro-α-iodoanisole (106261-89-6) → (E)-2-(4-chloro-phenyl)-ethenesulfonic acid (1,1,3,3-tetramethyl-butyl)-amide

Guidance literature:

With triethylamine; palladium diacetate; triphenylphosphine; In N,N-dimethyl-formamide; at 140 ℃; for 16h;

Reference yield: 45.0%

4-chloro-α-iodoanisole (106261-89-6) + propionyloxy>iodo>benzene → p-chlorophenoxymethyl 2-propionate (106262-04-8)

Guidance literature:

In dichloromethane; for 6h; Ambient temperature;

DOI:10.1039/P19860000795

upstream raw materials:

4-chloromethoxybenzene

Downstream raw materials:

p-chlorophenoxymethyl 2-propionate

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