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N,N'-dimethylisatinazine is an organic compound with the chemical formula C10H12N4. It is a derivative of isatinazine, a heterocyclic compound with a tricyclic structure consisting of a pyrazine ring fused to an indole ring. The N,N'-dimethylisatinazine specifically refers to the compound where two methyl groups are attached to the nitrogen atoms of the pyrazine ring. This modification can influence the compound's physical and chemical properties, such as solubility, reactivity, and potential applications in various fields, including pharmaceuticals and materials science. The compound is synthesized through chemical reactions and can be characterized by its molecular structure, which includes the presence of two methyl groups attached to the nitrogen atoms, altering the electronic properties and potentially the biological activity of the parent isatinazine molecule.

3265-17-6

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3265-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3265-17-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,6 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3265-17:
(6*3)+(5*2)+(4*6)+(3*5)+(2*1)+(1*7)=76
76 % 10 = 6
So 3265-17-6 is a valid CAS Registry Number.

3265-17-6Downstream Products

3265-17-6Relevant academic research and scientific papers

Reactivity of Carbenes and Related Compounds towards Molecular Nitrogen

Grieve, Duncan M. A.,Lewis, Graham E.,Ravenscroft, Michael D.,Skrabal, Peter,Sonoda, Takaaki,et al.

, p. 1427 - 1443 (2007/10/02)

The thermal N2 exchange of a number of 15N-labelled diazo compounds was studied in solution.The compounds involved were 3-diazo-1-methylindolin-2-one (1), 9-diazafluorene (2), 5-diazo-1,3-cyclopentadiene-1,2,3,4-tetracarbonitrile (3), 2-diazo-2H-imidazole-4,5-dicarbonitrile (4), 4-diazocyclohexa-2,5-dienone (5), and the conjugate acids of 4 and 5, namely 4,5-dicyano-1H-imidazole-2-diazonium ion (6) and 4-hydroxybenzenediazonium ion (7).Only 1, 4, 6, and 7 exchange their diazo group with 'external' molecular N2.The results are explained on the hypothesis that only organic species which have an empty ? orbital and which are effective in ? electron back-donation are able to react with N2.Thus, reaction with carbenes is likely to occur only if the carbene is in the 1A2 singlet state and if its electrophilicity is high.

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