128671-34-1

Basic information

• Product Name: 2-acetylphenyl (E)-2-(4-methoxyphenyl)acrylate
• Synonyms: 2-acetylphenyl (E)-2-(4-methoxyphenyl)acrylate
• CAS NO: 128671-34-1
• Molecular Weight: 296.323
• Mol File: 128671-34-1.mol

Chemical Properties

• CAS DataBase Reference: 2-acetylphenyl (E)-2-(4-methoxyphenyl)acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-acetylphenyl (E)-2-(4-methoxyphenyl)acrylate(128671-34-1)
• EPA Substance Registry System: 2-acetylphenyl (E)-2-(4-methoxyphenyl)acrylate(128671-34-1)

Safety Data

• Hazardous Substances Data: 128671-34-1(Hazardous Substances Data)

Upstream product

• 34446-64-5 (E)-3-(4-methoxyphenyl)propenoyl chloride 
• 118-93-4 o-hydroxyacetophenone 
• 830-09-1 3-(4'-methoxyphenyl)propenoic acid 
• 943-89-5 (E)-3-(4-methoxyphenyl)acrylic acid 

Downstream Products

• 51138-53-5 (E)-2-(4-methoxystyryl)-4H-chromen-4-one 
• 205308-05-0 (2Z,4E)-3-Hydroxy-1-(2-hydroxy-phenyl)-5-(4-methoxy-phenyl)-penta-2,4-dien-1-one 
• 128671-39-6 p-methoxy-2-cinnamoyloxy-ω-bromoacetophenone 

Relevant articles and documents

One-Pot Green Synthesis of 2-Hydroxybenzoyl(cinnamoyl)methanes and 2-Styrylchromones Using Dual-Frequency Ultrasonication

Abstract: One-pot green synthesis of (2-hydroxybenzoyl)(cinnamoyl)methanes has been performed by reacting 2-hydroxyacetophenones with cinnamoyl chlorides using activated Ba(OH)2, followed by Baker–Venkataraman rearrangement assisted by dual-fre

1,5-Diphenylpenta-2,4-dien-1-ones as potent and selective monoamine oxidase-B inhibitors

A series of (2E,4E)-1-(2-hydroxyphenyl)-5-phenylpenta-2,4-dien-1-ones (3a-r) and (2Z,4E)-3-hydroxy-1-(2-hydroxyphenyl)-5-phenylpenta-2,4-dien-1-ones (6a-l) were synthesized and evaluated in vitro as inhibitors of the two human Monoamine oxidase (hMAO) iso

Efficient syntheses of new polyhydroxylated 2,3-diaryl-9H-xanthen-9-ones

A large number of hydroxylated 2,3-diaryl-9/i-xanthen-9ones have been synthesised by two different approaches, starting either from 3-brom.o-2-m.elhyl-4H-ch:rom.en-4-one or from. (E)-3-brom.o-2-styryl-4H-chrom. en-4-ones. The former method involves Heck r

A novel and efficient route for the synthesis of hydroxylated 2,3-diarylxanthones

A novel, efficient and general route for the synthesis of hydroxylated 2,3-diarylxanthones is described. 3-Bromo-2-styryl-chromone, the key intermediate of this synthesis, is obtained by a Baker-Venkataraman rearrangement of the appropriate 2′-cinnamoylox

Synthesis of 4-Aryl-3-(2-chromonyl)-2-pyrazolines by the 1,3-Dipolar Cycloaddition of 2-Styrylchromones with Diazomethane

The first reported 1,3-dipolar cycloaddition of 2-styrylchromones with diazomethane afforded 4-aryl-3-(2-chromonyl)-2-pyrazolines. However, 3-aryl-4-(2-chromonyl)-1-pyrazolines have been also found as minor products of this reaction. These two series of p