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2-(4-nitrophenyl)-1H-imidazo[4,5-b]phenazine is a complex organic compound with the molecular formula C21H13N5O2. It is characterized by a phenazine core, which is a tricyclic system consisting of two fused benzene rings and one nitrogen atom. The imidazo[4,5-b]phenazine structure is formed by the fusion of an imidazole ring to the phenazine system. The compound is further distinguished by the presence of a 4-nitrophenyl group attached to the 2-position of the imidazo[4,5-b]phenazine. This nitro group confers additional reactivity and properties to the molecule, which can be significant in various chemical and biological contexts. The compound may be of interest in the fields of organic synthesis, medicinal chemistry, and materials science due to its unique structure and potential applications.

2870-64-6

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2870-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2870-64-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,7 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2870-64:
(6*2)+(5*8)+(4*7)+(3*0)+(2*6)+(1*4)=96
96 % 10 = 6
So 2870-64-6 is a valid CAS Registry Number.

2870-64-6Downstream Products

2870-64-6Relevant academic research and scientific papers

On the synthesis of pyrazino[2,3-b]phenazine and 1H-imidazo[4,5-b]phenazine derivatives

Amer, Atef M.,El-Bahnasawi, Adel A.,Mahran, Mohamed R.H.,Lapib, Mostafa

, p. 1217 - 1225 (1999)

Several pyrazino[2,3-b]pnenazine derivatives were prepared by the reaction of 2,3-diaminophenazine with different 1,2-diketones. Nucleophilic substitution of 2,3-dibromomethylpyrazino[2,3-b]phenazine with propanol, morpholine, and potassium thiocyanate gave 2,3-bis-(propoxymethyl )-pyrazino[2,3-b]phenazine, 2,3-bis-(4-morpholinylmethyl)-pyrazino[2,3-b]phenazine, and 2,3-bis-(cyanosulfanylmethyl)-pyrazino[2,3-b]phenazine, 2-Aryl-1H-imidazo[4,5-b]phenazine derivatives were synthesized by a one-pot reaction of 2,3-diaminophenazine with different aromatic aldehydes or acids. Reaction of 2,3-diaminophenazine with acetic anhydride and formic acid afforded 1H-imidazo [4,5-b]phenazine and 2-methyl-1H-imidazo[4,5-b]phenazine. Chemical and spectroscopic evidences for the product structures of the new compounds arc presented.

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