582311-53-3

Basic information

• Product Name: 2,5-Pyrrolidinedione, 1-[[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1-oxo-2-propenyl]oxy]-
• CAS NO: 582311-53-3
• Molecular Formula: C15H15NO7
• Molecular Weight: 321.287
• Mol File: 582311-53-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,5-Pyrrolidinedione, 1-[[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1-oxo-2-propenyl]oxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Pyrrolidinedione, 1-[[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1-oxo-2-propenyl]oxy]-(582311-53-3)
• EPA Substance Registry System: 2,5-Pyrrolidinedione, 1-[[(2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1-oxo-2-propenyl]oxy]-(582311-53-3)

Safety Data

• Hazardous Substances Data: 582311-53-3(Hazardous Substances Data)

Upstream product

• 6066-82-6 1-hydroxy-pyrrolidine-2,5-dione 
• 530-59-6 trans-3,5-dimethoxy-4-hydroxycinnamic acid 

Relevant articles and documents

THE PHOSPHOHYDROLYSIS OF HYDROXYCINNAMOYL-COENZIME A THIOESTERS IN PLANT EXTRACTS

In barley seedling extracts, p-coumaroyl-CoA is rapidly hydrolysed to p-coumaroyl-dephospho-CoA, p-coumaroyl-4'-phosphopantetheine and p-coumaroyl-pantetheine. p-Coumaroyl-4'-phosphopantetheine is active as a substrate of agmatine coumaroyl transferase in the formation of p-coumaroyl agmatine, but p-coumaroyl-pantetheine is inactive.The phosphohydrolysis can be partly inhibited by inorganic pyrophosphate, sodium fluoride and purine nucleotides.A simplified method for the synthesis of N-hydroxysuccinimide esters of hydroxycinnamic acids, used in the synthesis of CoA thioesters, is also described.Key Word Index -- Hordeum vulgare; Gramineae; barley seedlings; plant extracts; phosphohydrolysis; hydroxycinnamoyl-CoA; p-coumaroylagmatine.