32272-18-7

Basic information

• Product Name: 2-Propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(2-methoxyphenyl)-
• CAS NO: 32272-18-7
• Molecular Formula: C17H16O4
• Molecular Weight: 284.312
• Mol File: 32272-18-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(2-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(2-methoxyphenyl)-(32272-18-7)
• EPA Substance Registry System: 2-Propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(2-methoxyphenyl)-(32272-18-7)

Safety Data

• Hazardous Substances Data: 32272-18-7(Hazardous Substances Data)

Upstream product

• 90-02-8 salicylaldehyde 
• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 
• 135-02-4 ortho-anisaldehyde 
• 32274-70-7 2,2'-dihydroxy-4'-methoxy-trans-chalcone 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 1804-91-7 2'-benzyloxy-2,4'-dimethoxychalkone epoxide 
• 32272-17-6 7-methoxy-2-(2-methoxy-phenyl)-chroman-4-one 
• 1621-63-2 2'-benzyloxy-2,4'-dimethoxychalcone 
• 62536-78-1 7-methoxy-2-(2-methoxyphenyl)-4H-chromen-4-one 
• 77764-83-1 (Z)-6-methoxy-2-(2-methoxybenzylidene)benzofuran-3(2H)-one 
• 19725-40-7 7-methoxy-3-(2-methoxyphenyl)-4H-chromen-4-one 

Relevant articles and documents

Synthesis and Screening of Human Monoamine Oxidase-A Inhibitor Effect of New 2-Pyrazoline and Hydrazone Derivatives

A group of 3,5-diaryl-2-pyrazoline and hydrazone derivatives was prepared via the reaction of various chalcones with hydrazide compounds in ethanol. Twenty original compounds were synthesized. Ten of these original compounds have a pyrazoline structure, n

Synthesis and complete assignment of NMR data of 20 chalcones

Chalcones, intermediates in flavonoid biosynthesis, can exhibit antibacterial, antiproliferative, and anti-inflammatory properties. Chalcones contain two benzene rings and both hydroxylated and methoxylated analogs are frequently produced by hydroxylases and O-methyltransferases in plant biosynthetic pathways. Assignments of NMR peaks in the spectra of hydroxylated and/or methoxylated chalcones can help in identifying novel chalcone derivatives isolated from natural sources by referencing these data against NMR spectra obtained from known chalcones. We report here the syntheses of 20 chalcones and complete assignments of 1H and 13C NMR spectra. Copyright

Two Syntheses of 7,2'-Dimethoxyisoflavone

7,2'-Dimethoxyisoflavone (V) has been synthesised by two routes: (i) by direct oxidative rearrangement of 2'-hydroxy-2,4'-dimethoxychalkone; and (ii) by treatment of 2'-benzyloxy-2,4'-dimethoxychalkone epoxide (III) derivable from I, with BF3-etherate to