24043-40-1

Basic information

• Product Name: Propanedioic acid, [(4-methoxyphenyl)amino]-, diethyl ester
• CAS NO: 24043-40-1
• Molecular Formula: C14H19NO5
• Molecular Weight: 281.309
• Mol File: 24043-40-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Propanedioic acid, [(4-methoxyphenyl)amino]-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanedioic acid, [(4-methoxyphenyl)amino]-, diethyl ester(24043-40-1)
• EPA Substance Registry System: Propanedioic acid, [(4-methoxyphenyl)amino]-, diethyl ester(24043-40-1)

Safety Data

• Hazardous Substances Data: 24043-40-1(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 685-87-0 Diethyl 2-bromomalonate 

Downstream Products

• 221910-49-2 diethyl N-(4'-methoxyphenyl)-1-phenylthioacetyl-aminomalonate 
• 87542-26-5 (2S,3R)-1-(4-Methoxy-phenyl)-3-(2-methyl-[1,3]dioxolan-2-yl)-4-oxo-azetidine-2-carboxylic acid ethyl ester 
• 87542-26-5 (2R,3R)-1-(4-Methoxy-phenyl)-3-(2-methyl-[1,3]dioxolan-2-yl)-4-oxo-azetidine-2-carboxylic acid ethyl ester 
• 87542-25-4 1-(4-Methoxy-phenyl)-3-(2-methyl-[1,3]dioxolan-2-yl)-4-oxo-azetidine-2,2-dicarboxylic acid diethyl ester 
• 83304-70-5 3-Acetyl-1-(4-methoxy-phenyl)-4-oxo-azetidine-2,2-dicarboxylic acid diethyl ester 
• 106817-58-7 Diethyl N-bromoacetyl-N-(4-methoxyphenyl)-aminobromomalonate 
• 106817-59-8 3-Chloro-1-(4-methoxy-phenyl)-4-oxo-azetidine-2,2-dicarboxylic acid diethyl ester 
• 24043-42-3 diethyl 1-(4-methoxyphenyl)-4-oxoazetidine-2,2-dicarboxylate 
• 126737-05-1 1-(4-Methoxy-phenyl)-6-oxo-piperidine-2,2-dicarboxylic acid diethyl ester 
• 126737-06-2 2-[Butyryl-(4-methoxy-phenyl)-amino]-malonic acid diethyl ester 
• 126737-04-0 2-[(4-Methoxy-phenyl)-propionyl-amino]-malonic acid diethyl ester 
• 115026-82-9 2-[(3,3-Dimethyl-oxiranecarbonyl)-(4-methoxy-phenyl)-amino]-malonic acid diethyl ester 

Relevant articles and documents

A convenient synthesis of 3-phenylthio-azetidin-2-ones

3-Phenylthio-4,4-diethoxycarbonyl-azetidin-2-ones 8 have been conveniently synthesised by reacting 2-chlorophenylthioacetyl chloride 5 with aryl substituted aminomalonates 7 under mild basic conditions. Alternatively, C-3 alkylation of azetidin-2-one usin

Studies on beta-lactams.

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