1234363-56-4

Basic information

• Product Name: 1-(4-ethoxy-3-methoxyphenyl)prop-2-en-1-one
• Synonyms: 1-(4-ethoxy-3-methoxyphenyl)prop-2-en-1-one
• CAS NO: 1234363-56-4
• Molecular Weight: 206.241
• Mol File: 1234363-56-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(4-ethoxy-3-methoxyphenyl)prop-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-ethoxy-3-methoxyphenyl)prop-2-en-1-one(1234363-56-4)
• EPA Substance Registry System: 1-(4-ethoxy-3-methoxyphenyl)prop-2-en-1-one(1234363-56-4)

Safety Data

• Hazardous Substances Data: 1234363-56-4(Hazardous Substances Data)

Upstream product

• 203312-21-4 1-(4-ethoxy-3-methoxyphenyl)-2-(2-methoxy-phenoxy)propan-1,3-diol 
• 78405-40-0 1-(4-ethoxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethanol 
• 186255-41-4 1-(4-ethoxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethanone 
• 84159-64-8 4-ethoxy-3-methoxybromoacetylbenzene 
• 120-25-2 4-ethoxy-3-methoxybenzaldehyde 

Relevant articles and documents

SELECTIVE CARBON-CARBON BOND CLEAVAGE BY EARTH ABUNDANT VANADIUM COMPOUNDS UNDER VISIBLE LIGHT PHOTOCATALYSIS

Provided herein a vanadium(V) complex of formula I, where R1 to R8 are as defined herein. Also provided herein are reactions making use of the vanadium(V) complex of formula I, such as selective sp3-sp3 carbon-carbon bond cleavage under visible light photocatalysis and photodegradation of lignin.

CATALYTIC DISPROPORTIONATION AND CATALYTIC REDUCTION OF CARBON-CARBON AND CARBON-OXYGEN BONDS OF LIGNIN AND OTHER ORGANIC SUBSTRATES

The present invention provides methods and catalyst compositions for the catalytic reduction of carbon-oxygen bonds of organic substrates and the catalytic disproportionation of carbon-oxygen or carbon-carbon bonds of organic substrates. These methods and catalyst compositions may be used to depolymerize lignin. The disproportionation of carbon-oxygen or carbon-carbon bonds of organic substrates or lignin is carried out by cleaving a carbon-oxygen bond or a carbon-carbon bond in a catalytic disproportionation reaction. The catalysts may be formed from a metal precursor such as ruthenium or vanadium and a bidentate ligand The catalytic reduction of carbon-oxygen bonds of organic substrates such as lignin is carried out by cleaving a carbon-oxygen bond in the presence of a hydrogen atom source. Lignin fragments produced following depolymerization by such methods may be further processed into fuels.