75609-01-7

Basic information

• Product Name: ethyl p-nitrobenzoylazocarboxylate
• Synonyms: ethyl p-nitrobenzoylazocarboxylate
• CAS NO: 75609-01-7
• Molecular Weight: 251.199
• Mol File: 75609-01-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: ethyl p-nitrobenzoylazocarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl p-nitrobenzoylazocarboxylate(75609-01-7)
• EPA Substance Registry System: ethyl p-nitrobenzoylazocarboxylate(75609-01-7)

Safety Data

• Hazardous Substances Data: 75609-01-7(Hazardous Substances Data)

Upstream product

• 636-97-5 N-amino-(4-nitrophenyl)carboxamide 
• 23767-28-4 N-p-nitrobenzoyl-N'-ethoxycarbonyl hydrazine 

Downstream Products

• 619-80-7 4-nitrobenzamide 
• 86626-58-6 N-(2-Morpholin-4-yl-3-oxo-cyclohex-1-enyl)-N'-(4-nitro-benzoyl)-hydrazinecarboxylic acid ethyl ester 
• 86626-65-5 2-(morpholin-4-yl)-3-(5-p-nitrophenyl-1,3,4-oxadiazol-2(3H)-on-3-yl)cyclohex-2-en-1-one 
• 86626-70-2 2-(N-ethoxycarbonyl-N'-p-nitrobenzoyl)hydrazino-1,3-cyclohexadienone 
• 86626-62-2 2-hydroxy-6-(pyrrolidin-1-yl)phenylurethane 
• 55898-77-6 2-hydroxy-6-(morpholin-4-yl)phenylurethane 
• 80331-06-2 C₂₂H₂₉N₅O₁₀ 
• 80331-12-0 N-(5-tert-Butyl-2-oxo-cyclohexyl)-N'-(4-nitro-benzoyl)-hydrazinecarboxylic acid ethyl ester 
• 80331-11-9 N'-(4-Nitro-benzoyl)-N-(2-oxo-cyclohexyl)-hydrazinecarboxylic acid ethyl ester 
• 38864-15-2 6,7a-Dimethyl-1-(4-nitro-benzoyl)-3-(4-nitro-phenyl)-4a,5-diphenyl-4a,7a-dihydro-1H-cyclopenta[1,3,4]oxadiazin-7-one 
• 75609-12-0 6,7a-Dimethyl-3-(4-nitro-phenyl)-4a,5-diphenyl-4a,7a-dihydro-1H-cyclopenta[1,3,4]oxadiazin-7-one 
• 86626-53-1 N-(2-Morpholin-4-yl-6-oxo-cyclohex-1-enyl)-N'-(4-nitro-benzoyl)-hydrazinecarboxylic acid ethyl ester 
• 86626-57-5 4a-Morpholin-4-yl-3-(4-nitro-phenyl)-5-oxo-4a,5,6,7,8,8a-hexahydro-benzo[1,3,4]oxadiazine-1-carboxylic acid ethyl ester 
• 75609-02-8 cis-1-ethoxycarbonyl-3-p-nitrophenyl-6,7a-dimethyl-7-oxo-1,4a,7,7a-tetrahydrocyclopent<1,3,4>-oxadiazine 

Relevant articles and documents

1,3,4-OXADIAZINE DERIVATIVES FROM CYCLOHEXANONE ENAMINES AND ASYMMETRIC DIIMIDES; POSSIBILITY OF RING-CHAIN TAUTOMERISM IN SUCH HETEROCYCLIC SYSTEM

1,3,4-oxadiazine derivatives, in equilibrium with their corresponding trisubstituted enamine isomers, are obtained in a regiospecific way from cyclohexanone enamines and ethoxycarbonyl aroyl diimides.Such an equilibrium is not present in analogous oxadiazine systems, derived from aryl aroyl diimides.