132356-46-8

Basic information

• Product Name: 2H-1-Benzopyran-2-one, 3,3'-(3-phenyl-2-propenylidene)bis[4-hydroxy-, (E)-
• CAS NO: 132356-46-8
• Molecular Formula: C27H18O6
• Molecular Weight: 438.436
• Mol File: 132356-46-8.mol
• Article Data: 26

Chemical Properties

• CAS DataBase Reference: 2H-1-Benzopyran-2-one, 3,3'-(3-phenyl-2-propenylidene)bis[4-hydroxy-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-1-Benzopyran-2-one, 3,3'-(3-phenyl-2-propenylidene)bis[4-hydroxy-, (E)-(132356-46-8)
• EPA Substance Registry System: 2H-1-Benzopyran-2-one, 3,3'-(3-phenyl-2-propenylidene)bis[4-hydroxy-, (E)-(132356-46-8)

Safety Data

• Hazardous Substances Data: 132356-46-8(Hazardous Substances Data)

Upstream product

• 14371-10-9 (E)-3-phenylpropenal 
• 1076-38-6 4-hydroxy[1]benzopyran-2-one 
• 104-55-2 3-phenyl-propenal 

Downstream Products

• 138188-50-8 4-hydroxy-3-<3-phenyl(1-2H1)prop-2-enylidene>bis<-2H-1-benzopyran-2-one> 
• 6431-08-9 4-hydroxy-3-(3-phenylpropyl)-2H-1-benzopyran-2-one 
• 132356-66-2 (E)-4-hydroxy-3-(3-phenylallyl)chromen-2-one 
• 132356-60-6 (E)-4-methoxy-3-<1-(2-methoxy-4-oxo-4H-1-benzopyran-3-yl)-3-phenylprop-2-enyl>-2H-1-benzopyran-2-one 
• 132387-95-2 (E)-3,3'-(3-phenylprop-2-enylidene)bis<4-methoxy-2H-1-benzopyran-2-one> 

Relevant articles and documents

Biscoumarin: New class of urease inhibitors; Economical synthesis and activity

A variety of biscoumarins (1-21) with variable substituents at C-11 were synthesized with an improved method and evaluated as urease inhibitors. The synthesized compounds showed varying degree of urease inhibitory activity ranging from 15.06-91.35 μM. The size and electron donating or withdrawing effects of substituents influenced the activity, which lead to the urease inhibitors.

Heterogeneous SO3H@Fe3O4 magnetic nanocatalyst as an efficient and reusable medium for the synthesis of 3,3′-(arylmethylene)-bis-(4-hydroxycoumarin), bis-(indolyl)-methane, and 1,8-dioxo-octahydroxanthene derivatives

This work aimed to synthesize a new heterogeneous catalyst (SO3H@Fe3O4 magnetic nanoparticles) and the study of its catalytic behavior in synthesizing 3,3′-(arylmethylene)-bis-(4-hydroxycoumarin), bis-(indolyl)-methane, an

Investigation of catalytic, anti-bacterial, anti-oxidant, and DNA cleavage properties of bimetallic and trimetallic magnetic nanoalloys base on cupper

Bimetallic and trimetallic magnetic nanoalloys base on cupper were easily prepared from their starting materials. These nanoparticles (NPs) were used for the synthesis of biscoumarines by two-component one-pot domino Knoevenagel-type condensation/Michael