103344-71-4

Basic information

• Product Name: 2-Butenoic acid, 4-(4-chlorophenyl)-2-hydroxy-4-oxo-, (2Z)-
• CAS NO: 103344-71-4
• Molecular Formula: C10H7ClO4
• Molecular Weight: 226.616
• Mol File: 103344-71-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Butenoic acid, 4-(4-chlorophenyl)-2-hydroxy-4-oxo-, (2Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butenoic acid, 4-(4-chlorophenyl)-2-hydroxy-4-oxo-, (2Z)-(103344-71-4)
• EPA Substance Registry System: 2-Butenoic acid, 4-(4-chlorophenyl)-2-hydroxy-4-oxo-, (2Z)-(103344-71-4)

Safety Data

• Hazardous Substances Data: 103344-71-4(Hazardous Substances Data)

Upstream product

• 294624-23-0 (Z)-ethyl 4-(4-chlorophenyl)-2-hydroxy-4-oxo-2-butenoate 
• 99-91-2 para-chloroacetophenone 
• 39847-98-8 (Z)-methyl 4-(4-chlorophenyl)-2-hydroxy-4-oxobut-2-enoate 
• 58303-62-1 5-(4-chlorophenyl)-2,3-dihydrofuran-2,3-dione 

Downstream Products

• 1198396-87-0 C₂₁H₂₀ClNO₅S 
• 188935-75-3 4-(4-Chloro-phenyl)-3-[(4-chloro-phenyl)-hydrazono]-2,4-dioxo-butyric acid methyl ester 
• 188935-74-2 4-(4-Chloro-phenyl)-2,4-dioxo-3-(phenyl-hydrazono)-butyric acid methyl ester 
• 147670-98-2 5-(4-Chloro-benzoyl)-2-(4-chloro-phenyl)-2H-pyrazole-3,4-dione 
• 140939-06-6 5-(4-Chloro-benzoyl)-2-phenyl-2H-pyrazole-3,4-dione 
• 362623-40-3 4-(4-Chloro-phenyl)-3-[(4-chloro-phenyl)-hydrazono]-2,4-dioxo-butyric acid 
• 217474-43-6 4-(4-Chloro-phenyl)-2,4-dioxo-3-(phenyl-hydrazono)-butyric acid 

Relevant articles and documents

Diketo acids and their amino acid/dipeptidic analogues as promising scaffolds for the development of bacterial methionine aminopeptidase inhibitors

Using diketoesters as the template, various derivatives were designed and the selected compounds were synthesized as bacterial methionine aminopeptidase (MetAP) inhibitors. The results of in vitro antibacterial screening revealed fifteen compounds (1a-c,

CHEMISTRY OF OXALYL DERIVATIVES OF METHYL KETONES. XLII. RING OPENING IN 5-ARYL-2,3-DIHYDRO-2,3-FURANDIONES BY THE ACTION OF AROMATIC AMINES IN TOLUENE. EFFECT OF SUBSTITUENTS IN THE NUCLEOPHILIC REAGENTS AND SUBSTRATE ON THE RATE OF THE NONCATALYTIC REAC

The kinetics of the reactions of 5-aryl-2,3-dihydro-2,3-furandiones with aromatic amines were investigated by a spectrophotometric method.On the basis of an analysis of the dependence of the reaction rate on the nature of the substituents in the substrate