62080-95-9

Basic information

• Product Name: 2-Propen-1-one, 1-(3,4-dimethoxyphenyl)-2-(2-methoxyphenoxy)-
• CAS NO: 62080-95-9
• Molecular Formula: C18H18O5
• Molecular Weight: 314.338
• Mol File: 62080-95-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 1-(3,4-dimethoxyphenyl)-2-(2-methoxyphenoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 1-(3,4-dimethoxyphenyl)-2-(2-methoxyphenoxy)-(62080-95-9)
• EPA Substance Registry System: 2-Propen-1-one, 1-(3,4-dimethoxyphenyl)-2-(2-methoxyphenoxy)-(62080-95-9)

Safety Data

• Hazardous Substances Data: 62080-95-9(Hazardous Substances Data)

Upstream product

• 10535-17-8 1-(3,4-dimethoxyphenyl)-2-(methoxyphenoxy)propane-1,3-diol 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 10535-17-8 erythro-1-(3,4-dimethoxyphenyl)-2-(2-methoxyphenoxy)propane-1,3-diol 
• 93-03-8 (3,4-dimethoxyphenyl)methanol 
• 94687-10-2 ethyl-3-(3,4-dimethoxyphenyl)-3-hydroxy-2-(2-methoxyphenoxy)propanoate 
• 13078-21-2 ethyl 2-(2-methoxyphenoxy)acetate 
• 90-05-1 2-methoxy-phenol 
• 1131-62-0 1-(3,4-dimethoxyphenyl)ethanone 
• 32565-77-8 3-acetoxy-2-(2-methoxyphenoxy)-1-(3,4-dimethoxyphenyl)-1-propanone 
• 10548-77-3 1-(3,4-dimethoxyphenyl)-3-hydroxy-2-(2-methoxyphenoxy)propan-1-one 
• 22675-96-3 2-methoxyphenoxy-3',4'-dimethoxyacetophenone 
• 1835-02-5 2-Bromo-1-(3,4-dimethoxyphenyl)ethanone 
• 7572-96-5 1-(3,4-Dimethoxyphenyl)-2-carbethoxy-2-(2-methoxyphenoxy)ethanol 

Downstream Products

• 1835-04-7 ethyl 3,4-dimethoxyphenyl ketone 
• 90-05-1 2-methoxy-phenol 

Relevant articles and documents

METHOD OF SELECTIVELY OXIDIZING LIGNIN

A method of selectively reacting lignin or a lignin-derived reactant to yield an aromatic product. The method includes the step of reacting lignin or a lignin-derived reactant with a molybdenum-containing catalyst, in a solvent, and optionally in the presence of an oxidant, for a time and a temperature wherein at least a portion of the lignin or lignin-derived reactant is selectively converted into an aromatic product, preferably coniferaldehyde and/or sinapaldehyde.

SELECTIVE C-O BOND CLEAVAGE OF OXIDIZED LIGNIN AND LIGNIN-TYPE MATERIALS INTO SIMPLE AROMATIC COMPOUNDS

A method to cleave C-C and C-0 bonds in β-Ο-4 linkages in lignin or lignin sub-units is described. The method includes oxidizing at least a portion of secondary benzylic alcohol groups in β-Ο-4 linkages in the lignin or lignin sub-unit to corresponding ketones and then leaving C-0 or C-C bonds in the oxidized lignin or lignin sub-unit by reacting it with an organic carboxylic acid, a salt of an organic carboxylic acids, and/or an ester of an organic carboxylic acids. The method may utilize a metal or metal-containing reagent or proceed without the metal or metal-containing reagent.

SELECTIVE AEROBIC ALCOHOL OXIDATION METHOD FOR CONVERSION OF LIGNIN INTO SIMPLE AROMATIC COMPOUNDS

Described is a method to oxidize lignin or lignin sub-units. The method includes oxidation of secondary benzylic alcohol in the lignin or lignin sub-unit to a corresponding ketone in the presence of unprotected primarily aliphatic alcohol in the lignin or lignin sub-unit. The optimal catalyst system consists of HNO3 in combination with another Br?nsted acid, in the absence of a metal-containing catalyst, thereby yielding a selectively oxidized lignin or lignin sub-unit. The method may be carried out in the presence or absence of additional reagents including TEMPO and TEMPO derivatives.