1187923-23-4

Basic information

• Product Name: 1-methoxy-4-[1-(2-methylpropan-1-yloxy)ethyl]benzene
• Synonyms: 1-methoxy-4-[1-(2-methylpropan-1-yloxy)ethyl]benzene
• CAS NO: 1187923-23-4
• Molecular Weight: 208.301
• Mol File: 1187923-23-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-methoxy-4-[1-(2-methylpropan-1-yloxy)ethyl]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methoxy-4-[1-(2-methylpropan-1-yloxy)ethyl]benzene(1187923-23-4)
• EPA Substance Registry System: 1-methoxy-4-[1-(2-methylpropan-1-yloxy)ethyl]benzene(1187923-23-4)

Safety Data

• Hazardous Substances Data: 1187923-23-4(Hazardous Substances Data)

Upstream product

• 78-83-1 2-methyl-propan-1-ol 
• 3319-15-1 rac-1-(4-methoxyphenyl)-ethanol 
• 100-06-1 1-(4-methoxyphenyl)ethanone 

Relevant articles and documents

Direct synthesis of ethers from aldehydes and ketones. One-pot reductive etherification of benzaldehydes, alkyl aryl ketones, and benzophenones

Benzyl alcohols formed by the reduction of benzaldehydes, alkyl aryl ketones, and benzophenones with sodium tetrahydridoborate in alcohols undergo in situ etherification with the solvent in the presence of a catalytic amount of HCl. Thus the process may be regarded as one-pot transformation of carbonyl compounds into the corresponding benzyl ethers. The yields of ethers depend on the substituent nature in the aromatic fragment of the initial carbonyl compound and on the alcohol used as reduction medium.

Bifunctional copper catalysts for an atom efficient ether synthesis

A direct etherification of aromatic ketones and aliphatic alcohols into the corresponding asymmetrical ethers by the use of a bifunctional heterogeneous copper catalyst is described. The reaction protocol reveals to be versatile and convenient respect to the traditional ether synthesis for both environmental and practical concerns.