836-07-7

Basic information

• Product Name: 1-iodo-2-(4-methoxyphenoxy)benzene
• Synonyms: 1-iodo-2-(4-methoxyphenoxy)benzene
• CAS NO: 836-07-7
• Molecular Weight: 326.134
• Mol File: 836-07-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-iodo-2-(4-methoxyphenoxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-iodo-2-(4-methoxyphenoxy)benzene(836-07-7)
• EPA Substance Registry System: 1-iodo-2-(4-methoxyphenoxy)benzene(836-07-7)

Safety Data

• Hazardous Substances Data: 836-07-7(Hazardous Substances Data)

Upstream product

• 5720-07-0 4-methoxyphenylboronic acid 
• 129112-26-1 2-iodophenyltrifluoromethanesulfonic acid 
• 88-73-3 2-Chloronitrobenzene 
• 615-42-9 1,2-Diiodobenzene 
• 150-76-5 4-methoxy-phenol 
• 1493-27-2 ortho-nitrofluorobenzene 
• 105901-39-1 2-(4-Methoxyphenoxy)benzenamine 
• 58656-16-9 2-(4-methoxyphenoxy)nitrobenzene 
• 533-58-4 2-Iodophenol 
• 62790-87-8 4-(tert-butyldimethylsilyloxy)anisole 
• 348-52-7 1-Fluoro-2-iodobenzene 

Downstream Products

• 1379658-95-3 1-ethynyl-2-(4-methoxyphenoxy)benzene 
• 1379658-69-1 rac-(2-bromo-4-methylphenoxy)-4-(2-(4-methoxyphenoxy)phenyl)but-3-yn-2-ol 
• 1379658-94-2 ((2-(4-methoxyphenoxy)phenyl)ethynyl)trimethylsilane 
• 831-82-3 4-Phenoxyphenol 

Relevant articles and documents

Method for preparing 2-iodo aryl ether under action of alkali metal hydride

The invention discloses a method for preparing 2-iodo aryl ether under the action of alkali metal hydride, which comprises the following steps: adding alkali metal hydride and phenol into a solvent, then adding 1, 2-diiodo aromatic hydrocarbon, and reacti

Intramolecular Aryl Migration of Diaryliodonium Salts: Access to ortho-Iodo Diaryl Ethers

By using vicinal trifluoromethanesulfonate-substituted diaryliodonium salts, a novel approach was developed for the synthesis of ortho-iodo diaryl ethers by intramolecular aryl migration. The reaction conditions are mild with a broad substrate scope. Mechanistic insight suggests a sulfonyl-directed nucleophilic aromatic substitution pathway. Additionally, the product ortho-iodo diaryl ethers serve as versatile synthons as demonstrated with several coupling reactions. Furthermore, a useful thyroxine analogue of the 3-iodo-l-thyronine (3-T1) derivative was synthesized by this aryl migration procedure.

Copper-mediated N- and O-arylations with arylboronic acids in a continuous flow microreactor: a new avenue for efficient scalability

A continuous flow procedure has been elaborated for the copper(II)-mediated N- and O-arylation of a range of compounds with arylboronic acids using a commercial microreactor setup. The compounds could be continuously generated in good yields paving the way for efficient scalability.