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3H-indazol-3-ylidenediazenium, also known as 3H-indazole-3-ylidenediazenium, is a chemical compound with the molecular formula C7H6N3. It is a derivative of indazole, a heterocyclic aromatic compound consisting of a benzene ring fused to a pyrazole ring. The 3-ylidenediazenium group is attached to the indazole nucleus, which is characterized by the presence of a diazenium ion (N=N+) and a hydrogen atom at the 3-position. 3H-indazol-3-ylidenediazenium is of interest in the field of organic chemistry, particularly in the synthesis of various indazole-based compounds with potential applications in pharmaceuticals, agrochemicals, and materials science. The reactivity and properties of 3H-indazol-3-ylidenediazenium are influenced by the presence of the diazenium group, which can participate in various chemical reactions, such as coupling and cycloaddition processes.

2596-89-6

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2596-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2596-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,9 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2596-89:
(6*2)+(5*5)+(4*9)+(3*6)+(2*8)+(1*9)=116
116 % 10 = 6
So 2596-89-6 is a valid CAS Registry Number.

2596-89-6Relevant academic research and scientific papers

Reactions with Diazoazoles, VII. 3H-Azolo-1,2,4-triazoles by 1,8- or 1,12-Electrocyclizations of 3H-Pyrazol-3-one- or 3H-Indazol-3-one (Diorganylmethylene)hydrazones, Respectively

Ege, Guenter,Gilbert, Karlheinz,Heck, Reinhard

, p. 1726 - 1747 (2007/10/02)

3H-Azolo-1,2,4-triazoles 3 are formed by cycloreactions of diazoazoles 1 with diazoalkanes 2 and with fluorene-N-,P-,S-ylides 4, respectively, (Method A) or by cyclizing dehydrogenation of diorganylmethanone (1H-azol-3-yl)hydrazones 7 (Method B).In both m

Reactions with Diazoazoles. Part IV. (1). - and -Cyclocondensation Reactions of Diazoazoles with Acyltriphenylphosphonium Methylides to Azolotriazines

Ege, Guenter,Gilbert, Karlheinz

, p. 675 - 677 (2007/10/02)

Acyltriphenylphosphoniummethylides react with diazoazoles in a - or -cycloaddition reaction followed by elimination of triphenylphosphane oxide to yield azolotriazines.

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