99634-01-2

Basic information

• Product Name: 3-hydroxy-2-(2-methoxyphenoxy)-1-phenyl-1-propanone
• Synonyms: 3-hydroxy-2-(2-methoxyphenoxy)-1-phenyl-1-propanone
• CAS NO: 99634-01-2
• Molecular Weight: 272.301
• Mol File: 99634-01-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-hydroxy-2-(2-methoxyphenoxy)-1-phenyl-1-propanone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-hydroxy-2-(2-methoxyphenoxy)-1-phenyl-1-propanone(99634-01-2)
• EPA Substance Registry System: 3-hydroxy-2-(2-methoxyphenoxy)-1-phenyl-1-propanone(99634-01-2)

Safety Data

• Hazardous Substances Data: 99634-01-2(Hazardous Substances Data)

Upstream product

• 227300-29-0 2-(2-methoxyphenoxy)-1-phenylpropane-1,3-diol 
• 19513-80-5 2-(2-methoxyphenoxy)-1-(4-methoxyphenyl)ethan-1-one 
• 92409-23-9 3-hydroxy-2-(2-methoxyphenoxy)-1-(4-methoxyphenyl)propan-1-one 
• 90-05-1 2-methoxy-phenol 
• 70-11-1 α-bromoacetophenone 
• 22675-96-3 2-methoxyphenoxy-3',4'-dimethoxyacetophenone 
• 92409-15-9 2-(2-methoxyphenoxy)-1-(4-methoxyphenyl)-1-hydroxy-3-propanol 
• 17078-88-5 1-(3,4-dimethoxyphenyl)-2-(2-methoxyphenoxy)ethanol 
• 10535-17-8 1-(3,4-dimethoxyphenyl)-2-(methoxyphenoxy)propane-1,3-diol 
• 50-00-0 formaldehyd 
• 14385-48-9 2-(2-methoxyphenoxy)-acetophenone 

Downstream Products

• 1252675-90-3 1-(4-benzoyloxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethanone 
• 90-05-1 2-methoxy-phenol 
• 98-86-2 acetophenone 
• 98-85-1 1-Phenylethanol 
• 14385-48-9 2-(2-methoxyphenoxy)-acetophenone 
• 7382-68-5 1-(4-hydroxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethanol 
• 22317-35-7 1-(4-hydroxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethan-1-one 
• 38768-62-6 methyl (2-methoxyphenoxy) ethanoate 
• 1400880-11-6 C₅₆H₄₄O₆P₂Ru 
• 1400880-13-8 C₄₉H₃₈O₄P₂Ru 
• 227300-29-0 2-(2-methoxyphenoxy)-1-phenylpropane-1,3-diol 
• 17078-88-5 1-(3,4-dimethoxyphenyl)-2-(2-methoxyphenoxy)ethanol 
• 22675-96-3 2-methoxyphenoxy-3',4'-dimethoxyacetophenone 

Relevant articles and documents

Cleavage∕cross-coupling strategy for converting β-O-4 linkage lignin model compounds into high valued benzyl amines via dual C–O bond cleavage

Lignin is the most recalcitrant of the three components of lignocellulosic biomass. The strength and stability of the linkages have long been a great challenge for the degradation and valorization of lignin biomass to obtain bio-fuels and commercial chemicals. Up to now, the selective cleavage of C–O linkages of lignin to afford chemicals contains only C, H and O atoms. Our group has developed a cleavage/cross-coupling strategy for converting 4-O-5 linkage lignin model compounds into high value-added compounds. Herein, we present a palladium-catalyzed cleavage/cross-coupling of the β-O-4 lignin model compounds with amines via dual C–O bond cleavage for the preparation of benzyl amine compounds and phenols.

Selective Cα Alcohol Oxidation of Lignin Substrates Featuring a β-O-4 Linkage by a Dinuclear Oxovanadium Catalyst via Two-Electron Redox Processes

Developing highly efficient catalyst systems to transform lignin biomass into value-added chemical feedstocks is imperative for utilizing lignin as renewable alternatives to fossil fuels. Recently, the pre-activated strategy involving the selective oxidat