75907-18-5

Basic information

• Product Name: Propanedioic acid, (4-methoxybenzoyl)-, diethyl ester
• CAS NO: 75907-18-5
• Molecular Formula: C15H18O6
• Molecular Weight: 294.304
• Mol File: 75907-18-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Propanedioic acid, (4-methoxybenzoyl)-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanedioic acid, (4-methoxybenzoyl)-, diethyl ester(75907-18-5)
• EPA Substance Registry System: Propanedioic acid, (4-methoxybenzoyl)-, diethyl ester(75907-18-5)

Safety Data

• Hazardous Substances Data: 75907-18-5(Hazardous Substances Data)

Upstream product

• 201230-82-2 carbon monoxide 
• 5720-07-0 4-methoxyphenylboronic acid 
• 105-53-3 diethyl malonate 
• 137786-67-5 ethyl 3-amino-2-ethoxycarbonyl-2-butenoate 
• 570-08-1 diethyl acetylmalonate 
• 100-07-2 4-methoxy-benzoyl chloride 
• 123-54-6 acetylacetone 
• 75907-21-0 2-[Hydroxy-(4-methoxy-phenyl)-methylene]-malonic acid diethyl ester 

Downstream Products

• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 23982-31-2 7-hydroxy-4-(4-methoxyphenyl)-2H-chromen-2-one 
• 7394-23-2 p-Brom-benzolsulfonsaeure-<1-p-anisoyl-2,2-diaethoxycarbonyl-vinylester> 
• 75907-21-0 2-[Hydroxy-(4-methoxy-phenyl)-methylene]-malonic acid diethyl ester 
• 370582-94-8 7,8-dihydroxy-4-(4-methoxyphenyl)-2H-chromen-2-one 

Relevant articles and documents

Efficient synthesis of 4-ethoxycarbonyl pyrazolin-5-one derivatives

Concise and efficient methods for the preparation of 3-substituted 4-ethoxycarbonylpyrazolin-5-ones are described. The synthetic strategies involve carbon-acylation in the presence of base, followed by ring cyclization with hydrazine or hydrazine monohydrochloride.

Pd-catalyzed carbonylation for the construction of tertiary and quaternary carbon centers with sp3 carbon partners

The first examples of a Pd-catalyzed carbonylation of aryl boronic acids with sp3 carbon partners are presented. Various boronic acids were shown to react with 1,3-diesters and 1,3-diketones to afford structurally unique carbonyl compounds. By

TRANSMISSION OF SUBSTITUENT EFFECTS IN PARA SUBSTITUTED BENZOYLMALONATE DERIVATIVES

Acidity constants and enol contents of ethyl benzoylmalonate and its para derivatives (CH3O, CH3, Cl, CN, NO2) were determined in 75 vol.percent ethanol-water solutions.Acidity constants of keto and enol forms were calculated and correlated with substituents constants ?p.IR spectra and enol contents were also determined in CCl4 solutions.