155568-39-1

Basic information

• Product Name: diethyl 2-malonate
• Synonyms: diethyl 2-malonate
• CAS NO: 155568-39-1
• Molecular Weight: 404.379
• Mol File: 155568-39-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: diethyl 2-malonate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl 2-malonate(155568-39-1)
• EPA Substance Registry System: diethyl 2-malonate(155568-39-1)

Safety Data

• Hazardous Substances Data: 155568-39-1(Hazardous Substances Data)

Upstream product

• 6829-40-9 aminomalonic acid diethyl ester 
• 69195-96-6 5-nitro-1-(phenylmethyl)-1H-imidazole-4-carboxylic acid 

Downstream Products

• 155568-48-2 diethyl 2-methoxy-2-malonate 
• 155568-41-5 3-benzyl-6-ethoxycarbonyl-4,5,7,8-tetrahydro-6H-imidazo<4,5-e><1,4>diazepine-5,8-dione 
• 155568-42-6 3-benzyl-4,5,7,8-tetrahydro-6-methoxycarbonyl-6H-imidazo<4,5-e><1,4>diazepine-5,8-dione 
• 159530-80-0 6-Amino-3-benzyl-5,8-dioxo-3,4,5,6,7,8-hexahydro-imidazo[4,5-e][1,4]diazepine-6-carboxylic acid methyl ester 
• 155568-57-3 diethyl 2-methoxy-2-malonate 
• 159530-79-7 diethyl 2-benzylamino-2-malonate 
• 155568-55-1 3-benzyl-4,5,7,8-tetrahydro-6-methoxy-6-methoxycarbonyl-6H-imidazo<4,5-e><1,4>diazepine-5,8-dione 
• 324750-70-1 diethyl 2-phthalimido-2-[N-(5-amino-1-benzylimidazolyl-4-carbonyl)amino]malonate 
• 324750-69-8 diethyl 2-phthalimido-2-[N-(1-benzyl-5-nitroimidazolyl-4-carbonyl)amino]malonate 
• 159530-78-6 diethyl 2-benzylamino-2-malonate 

Relevant articles and documents

Analogues of azepinomycin: Inhibitors of guanase

Synthesis and guanase inhibitory activity of two novel 5:7-fused heterocyles, 15 and 16, containing the imidazo[4,5-e][1,4]diazepine ring system, have been reported.

A model study for a novel synthetic approach to 2-carboxyinosines

A model study for a novel approach to the synthesis of 2-carboxyinosines has been described. The synthesis of 9-benzyl-2-carboxyhypoxanthine (I), a model for 2-carboxyinosine, was achieved in four steps starting from 1-benzyl-5-nitroimidazole-4-carboxylic acid. Also reported is the synthesis of 9-benzyl-2,2-bis(ethoxycarbonyl)hypoxanthine (II). (C) 2000 Elsevier Science Ltd.