61023-54-9

Basic information

• Product Name: Propanedioic acid, [(2,4-dichlorophenyl)methyl]-, diethyl ester
• CAS NO: 61023-54-9
• Molecular Formula: C14H16Cl2O4
• Molecular Weight: 319.185
• Mol File: 61023-54-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Propanedioic acid, [(2,4-dichlorophenyl)methyl]-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanedioic acid, [(2,4-dichlorophenyl)methyl]-, diethyl ester(61023-54-9)
• EPA Substance Registry System: Propanedioic acid, [(2,4-dichlorophenyl)methyl]-, diethyl ester(61023-54-9)

Safety Data

• Hazardous Substances Data: 61023-54-9(Hazardous Substances Data)

Upstream product

• 94-99-5 2,4-Dichlorobenzyl chloride 
• 105-53-3 diethyl malonate 
• 15725-40-3 diethyl 2-(2,4-dichlorobenzylidene)malonate 

Downstream Products

• 1351601-09-6 1-(2,4-dichloro-phenyl)-3-hydroxy-propan-2-one O-methyl-oxime 
• 1351601-29-0 3-(2,4-dichloro-phenyl)-2-(hydroxyimino)-propionic acid methyl ester 
• 1351601-30-3 3-(2,4-dichloro-phenyl)-2-(methoxyimino)-propionic acid methyl ester 
• 448193-94-0 5,7-dichloro-2,3-dihydro-1H-inden-1-one 
• 5472-68-4 rac-2,4-dichloro-Phe 
• 66648-64-4 4-(2,4-dichlorophenyl)butanoic acid 
• 146882-06-6 (2,4-dichloro-benzyl)-malonic acid 
• 55144-92-8 3-(2,4-dichlorophenyl)propionic acid 

Relevant articles and documents

Synthesis and insecticidal activity of mesoionic pyrido[1,2-α]pyrimidinone derivatives containing a neonicotinoid moiety

Mesoionic pyrido[1,2-α]pyrimidinone derivatives containing a neonicotinoid moiety were designed, synthesized, and evaluated for their insecticidal activity. Some of the title compounds showed remarkable insecticidal properties against Aphis craccivora. Compound I13 exhibited satisfactory insecticidal activity against A. craccivora. Meanwhile, label-free proteomics analysis of compound I13 treatment identified a total of 821 proteins. Of these, 35 proteins were up-regulated, whereas 108 proteins were down-regulated. Differential expressions of these proteins reflected a change in cellular structure and metabolism.

Reactions of N-Substituted Pyridinium Cations with Carbanions: 5,6,8,9-Tetrahydro-7-phenylbisbenzoacridine, a Superior Leaving Group

N-Substituents are transferred from pyridinium cations to malonate, cyanoacetate , and acetoacetate carbanions: for alkyl substituents the pentacyclic derivatives (4) attain the required activity.