4496-29-1

Basic information

• Product Name: 1H-Naphth[2,3-d]imidazole-4,9-dione, 2-phenyl-
• CAS NO: 4496-29-1
• Molecular Formula: C17H10N2O2
• Molecular Weight: 274.279
• Mol File: 4496-29-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1H-Naphth[2,3-d]imidazole-4,9-dione, 2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Naphth[2,3-d]imidazole-4,9-dione, 2-phenyl-(4496-29-1)
• EPA Substance Registry System: 1H-Naphth[2,3-d]imidazole-4,9-dione, 2-phenyl-(4496-29-1)

Safety Data

• Hazardous Substances Data: 4496-29-1(Hazardous Substances Data)

Upstream product

• 117-80-6 2,3-Dichloro-1,4-naphthoquinone 
• 618-39-3 benzamidin 
• 13755-95-8 2,3-diamino-1,4-naphthoquinone 
• 100-52-7 benzaldehyde 
• 5292-53-5 diethyl benzalmalonate 

Relevant articles and documents

Synthesis of 2-aryl-1-hydroxy-1H-naphtho[2,3-d]imidazole-4,9-diones by reaction of 2-benzylamino-1,4-naphthoquinones with nitric acid

2-Aryl-1-hydroxy-1H-naphtho[2,3-d]imidazole-4,9-diones were synthesized by treatment of 2-benzylamino-1,4-naphthoquinones with a mixture of nitric and sulfuric acids in acetic acid.

Tuning of the H-bonding ability of imidazole N-H towards the colorimetric sensing of fluoride and cyanide ions as their sodium salts in water

Imidazole functionalized receptors, 2-R-1H-naphtho[2,3-d]imidazole-4,9- dione (2a-h), containing naphthoquinone as a chromogenic signalling unit have been synthesized from the reaction of 2,3-diaminonaphthoquinone and different aldehydes. These receptors

Use of tricyclic derivatives of 1,4-dihydro-1,4-dioxo-1H-naphthalene, novel compounds obtained and their application in theraphy

The invention concerns the therapeutic use of tricyclic salts and their pharmaceutically acceptable salts having the general formula: in which: A is either a sulfur atom, an oxygen atom, or an R3N radical where R3is a hydrogen atom,