95276-54-3

Basic information

• Product Name: cyano-2 oxo-5 diphenyl-3,5 pentanoate de methyle
• CAS NO: 95276-54-3
• Molecular Weight: 307.349
• Mol File: 95276-54-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: cyano-2 oxo-5 diphenyl-3,5 pentanoate de methyle(CAS DataBase Reference)
• NIST Chemistry Reference: cyano-2 oxo-5 diphenyl-3,5 pentanoate de methyle(95276-54-3)
• EPA Substance Registry System: cyano-2 oxo-5 diphenyl-3,5 pentanoate de methyle(95276-54-3)

Safety Data

• Hazardous Substances Data: 95276-54-3(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 79-20-9 acetic acid methyl ester 
• 861317-48-8 2-benzoyl-1-cyano-3-phenyl-cyclopropanecarboxylic acid methyl ester 
• 94-41-7 benzalacetophenone 
• 105-34-0 methyl 2-cyanoacetate 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 124-41-4 sodium methylate 

Downstream Products

• 89649-52-5 3,5-diphenylpyrrole-2-carboxylate de methyle 
• 1148157-87-2 methyl 3,5-diphenylthiophene-2-carboxylate 
• 1373319-68-6 methyl 1-benzyl-3,5-diphenyl-1H-pyrrole-2-carboxylate 
• 1373319-67-5 C₃₁H₂₆N₂O 
• 861317-48-8 2-benzoyl-1-cyano-3-phenyl-cyclopropanecarboxylic acid methyl ester 
• 85936-84-1 benzoyl-4 phenyl-3 butyro nitrile 
• 94905-50-7 2-oxo-4,6-diphenyl-1,2,3,4-tetrahydro-pyridine-3-carboxylic acid 
• 5456-53-1 5-oxo-3,5-diphenylpentanoic acid 
• 861324-43-8 2,4-dibromo-2-cyano-5-oxo-3,5-diphenyl-valeric acid methyl ester 
• 116597-46-7 2-cyano-5-oxo-2-(3-oxo-1,3-diphenyl-propyl)-3,5-diphenyl-valeric acid methyl ester 
• 861310-92-1 2-bromo-2-cyano-5-oxo-3,5-diphenyl-valeric acid methyl ester 
• 93729-27-2 2-cyano-5-oxo-3,5-diphenyl-valeric acid 
• 332072-07-8 2-bromo-4,6-diphenyl-nicotinic acid methyl ester 
• 1292310-23-6 methyl 2,5-dioxo-3,5-diphenylpentanoate 

Relevant articles and documents

An active and selective heterogeneous catalytic system for Michael addition

Potassium fluoride doped natural zeolite was found to be an efficient and selective solid base catalyst for 1,4-Michael addition. The catalyst is easily prepared and the workup procedure simplified by simple filtration. All products were obtained in high

Construction of 1,2,5-tricarbonyl compounds using methyl cyanoacetate as a glyoxylate anion synthon combined with copper(I) iodide-catalyzed aerobic oxidation

A practical and efficient synthesis of various 1,2,5-tricarbonyl compounds is described. The synthesis has been carried out by a conjugate addition of methyl cyanoacetate to the β-position of α,β-unsaturated carbonyl compounds and a subsequent copper(I) iodide-catalyzed aerobic oxidation. In addition, various α-aryl- and α-alkyl-α-keto esters have been synthesized using a similar approach. Copyright

Michael additions of methylene active compounds to chalcone in ionic liquids without any catalyst: The peculiar properties of ionic liquids

Michael additions of malonodinitrile as well as several other reagents to chalcone have been found to proceed well in pure ionic liquids, without the addition of any catalyst. The catalytic effect of the residual acidity caused by hydrolysis of ionic liqu