1655-72-7

Basic information

• Product Name: 1-(4-Methoxyphenoxy)-2-methoxybenzene
• Synonyms: 1-(4-Methoxyphenoxy)-2-methoxybenzene;1-Methoxy-2-(4-methoxyphenoxy)benzene;Benzene, 1-Methoxy-2-(4-Methoxyphenoxy)-
• CAS NO: 1655-72-7
• Molecular Formula: C₁₄H₁₄O₃
• Molecular Weight: 230.26
• Mol File: 1655-72-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(4-Methoxyphenoxy)-2-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-Methoxyphenoxy)-2-methoxybenzene(1655-72-7)
• EPA Substance Registry System: 1-(4-Methoxyphenoxy)-2-methoxybenzene(1655-72-7)

Safety Data

• Hazardous Substances Data: 1655-72-7(Hazardous Substances Data)

Usage

General Description

1-(4-Methoxyphenoxy)-2-methoxybenzene, also known as Anisole, is a chemical compound with the molecular formula C14H14O3. It is a colorless liquid that is commonly used as a precursor in the synthesis of various organic compounds. Anisole is often utilized as a solvent in various chemical reactions and is also found in some fragrances and perfumes. It has a sweet, pleasant odor and is flammable, making it important to handle with care. Anisole is also used in the production of pharmaceuticals, agrochemicals, and dyes, making it a versatile and valuable chemical compound in various industries.

Upstream product

• 104-92-7 1-bromo-4-methoxy-benzene 
• 5633-98-7 potassium guaiacolate 
• 14064-92-7 2,4'-dimethoxy-5-nitrodiphenyl ether 
• 14064-87-0 4'-Methoxy-5-nitro-2-hydroxy-diphenylaether 
• 6698-71-1 p-acetonyloxyanisole 
• 90-05-1 2-methoxy-phenol 
• 578-57-4 2-bromoanisole 
• 150-76-5 4-methoxy-phenol 
• 5720-07-0 4-methoxyphenylboronic acid 
• 14064-97-2 2,4'-Dimethoxy-5-amino-diphenylaether 

Downstream Products

• 150-76-5 4-methoxy-phenol 
• 90-05-1 2-methoxy-phenol 

Relevant articles and documents

Ullmann diaryl ether synthesis: rate acceleration by 2,2,6,6-tetramethylheptane-3,5-dione.

[reaction: see text]. In the copper salt catalyzed ether formation from aryl bromides or iodides and phenols, 2,2,6,6-tetramethylheptane-3,5-dione (TMHD) was found to greatly accelerate the ordinarily difficult reaction, making it occur under more moderate temperatures and reaction times. A series of aryl halides and phenols were shown to form ethers in NMP as the solvent, cesium carbonate as the base, and CuCl and TMHD as the catalysts. The reaction was shown to tolerate electron-rich aryl bromides and electron-neutral phenols.

Synthesis of diaryl ethers through the copper-promoted arylation of phenols with arylboronic acids. An expedient synthesis of thyroxine

Diaryl ethers are readily synthesized in high yield at room temperature through the copper(II)-promoted coupling of arylboronic acids and phenols. The reaction is tolerant of a wide range of substituents on both coupling partners. These reaction condition