94059-15-1

Basic information

• Product Name: Benzoic acid, 4-nitro-, 2-(4-hydroxy-3,6-dioxo-5-undecyl-1,4-cyclohexadien-1-yl)hydrazide
• CAS NO: 94059-15-1
• Molecular Formula: C24H31N3O6
• Molecular Weight: 457.527
• Mol File: 94059-15-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-nitro-, 2-(4-hydroxy-3,6-dioxo-5-undecyl-1,4-cyclohexadien-1-yl)hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-nitro-, 2-(4-hydroxy-3,6-dioxo-5-undecyl-1,4-cyclohexadien-1-yl)hydrazide(94059-15-1)
• EPA Substance Registry System: Benzoic acid, 4-nitro-, 2-(4-hydroxy-3,6-dioxo-5-undecyl-1,4-cyclohexadien-1-yl)hydrazide(94059-15-1)

Safety Data

• Hazardous Substances Data: 94059-15-1(Hazardous Substances Data)

Upstream product

• 550-24-3 embelin 
• 636-97-5 N-amino-(4-nitrophenyl)carboxamide 

Downstream Products

• 94059-30-0 Acetic acid 7-acetoxy-1-acetyl-3-(4-nitro-phenyl)-5-undecyl-1H-benzo[1,3,4]oxadiazin-6-yl ester 
• 116222-31-2 8-Nitro-3-(4-nitro-phenyl)-5-undecyl-1H-4-oxa-1,2,6,11-tetraaza-naphthacene 
• 116222-34-5 8,10-Dibromo-3-(4-nitro-phenyl)-5-undecyl-1H-4-oxa-1,2,6,11-tetraaza-naphthacene 
• 116222-35-6 10-Bromo-8-methyl-3-(4-nitro-phenyl)-5-undecyl-1H-4-oxa-1,2,6,11-tetraaza-naphthacene 
• 116222-33-4 8-Bromo-3-(4-nitro-phenyl)-5-undecyl-1H-4-oxa-1,2,6,11-tetraaza-naphthacene 
• 116222-32-3 8-Methyl-3-(4-nitro-phenyl)-5-undecyl-1H-4-oxa-1,2,6,11-tetraaza-naphthacene 
• 116222-30-1 3-(4-Nitro-phenyl)-5-undecyl-1H-4-oxa-1,2,6,11-tetraaza-naphthacene 
• 116222-28-7 4-Nitro-benzoic acid N'-(7,9-dibromo-3-hydroxy-4-undecyl-phenazin-2-yl)-hydrazide 
• 116222-27-6 4-Nitro-benzoic acid N'-(7-bromo-3-hydroxy-4-undecyl-phenazin-2-yl)-hydrazide 
• 116222-25-4 4-Nitro-benzoic acid N'-(3-hydroxy-7-nitro-4-undecyl-phenazin-2-yl)-hydrazide 
• 116222-24-3 4-Nitro-benzoic acid N'-(3-hydroxy-4-undecyl-phenazin-2-yl)-hydrazide 
• 116222-26-5 4-Nitro-benzoic acid N'-(3-hydroxy-7-methyl-4-undecyl-phenazin-2-yl)-hydrazide 
• 116222-29-8 4-Nitro-benzoic acid N'-(9-bromo-3-hydroxy-7-methyl-4-undecyl-phenazin-2-yl)-hydrazide 

Relevant articles and documents

Synthesis of 6,7-dihydroxy-3-aryl-5-undecyl-4,1,2-benzoxadiazines

Condensation of Embelin 1 with different aromatic acid hydrazides 2 in glacial acetic acid to give N1-5-hydroxy-6-undecyl-pbcnzoaquinone-2- yl)-benzohydrides 3. Reductive cyclization of the product 3 with simultaneous acetylation in situ resulted in the formation of the compound 4 l-N-acetyl-6,7-diacetyl-3-aryl-5-undccyl-4,1,2-benzoxadiazine. In the final step the compound 4 is deacetylated to give the title products 5. The structures of the newly prepared compounds have been confirmed from analytical and spectral data. Some of the compounds exhibited antibacterial and antifungal activity.