324025-34-5

Basic information

• Product Name: 2-[1-(4-methoxyphenyl)-3-oxo-3-phenylpropyl]-malonic acid dimethyl ester
• Synonyms: 2-[1-(4-methoxyphenyl)-3-oxo-3-phenylpropyl]-malonic acid dimethyl ester
• CAS NO: 324025-34-5
• Molecular Weight: 370.402
• Mol File: 324025-34-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-[1-(4-methoxyphenyl)-3-oxo-3-phenylpropyl]-malonic acid dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[1-(4-methoxyphenyl)-3-oxo-3-phenylpropyl]-malonic acid dimethyl ester(324025-34-5)
• EPA Substance Registry System: 2-[1-(4-methoxyphenyl)-3-oxo-3-phenylpropyl]-malonic acid dimethyl ester(324025-34-5)

Safety Data

• Hazardous Substances Data: 324025-34-5(Hazardous Substances Data)

Upstream product

• 22252-15-9 trans-4-methoxychalcone 
• 108-59-8 malonic acid dimethyl ester 
• 105-53-3 diethyl malonate 
• 959-33-1 3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one 

Relevant articles and documents

Layered double hydroxides-supported diisopropylamide: Synthesis, characterization and application in organic reactions

The layered double hydroxides-supported diisopropylamide (LDH-DA) catalyst is found to be an efficient and selective solid base for aldol, Knoevenagel, Henry, Michael, transesterification and epoxidation reactions under liquid phase conditions. LDH-DA is synthesized by the interaction of lithium diisopropylamide with LDH-NO3 (as-synthesized) and calcined LDH-NO3. The LDH-DA (Mg/Al, 3/1) and their precursors are well characterized by using various instrumental techniques such as FT-IR, TGA and DTA, powder XRD, solid state 27Al MAS NMR spectroscopy, SEM and XPS (ESCA).

Chiral bisphosphazides as dual basic enantioselective catalysts

Chiral bisphosphazides complexed with lithium salts efficiently catalyze the direct enantioselective 1,4-addition of dialkyl malonates to acyclic enones. Spectroscopic studies on the stoichiometry of the bisphosphazide and lithium salt have indicated the

Magnesium-lanthanum mixed metal oxide: A strong solid base for the michael addition reaction

Michael additions were achieved quantitatively at room temperature with a broad spectrum of acceptors and donors, using a magnesium-lanthanum mixed oxide, a strong solid base. The best solvent for the reaction is dimethylformamide, but good yields were al