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1H-1,2,3-Triazole, 1,5-dimethyl- is an organic compound with the chemical formula C4H7N3. It is a derivative of the 1,2,3-triazole ring system, which is a five-membered heterocyclic ring containing three nitrogen atoms. The 1,5-dimethyl substitution refers to the presence of two methyl groups (CH3) attached to the 1st and 5th positions of the triazole ring. 1H-1,2,3-Triazole, 1,5-dimethyl- is known for its stability and is often used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other chemical compounds due to its unique reactivity and properties. It is also recognized for its potential applications in materials science, such as in the development of new polymers and coatings.

15922-53-9

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15922-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15922-53-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,2 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15922-53:
(7*1)+(6*5)+(5*9)+(4*2)+(3*2)+(2*5)+(1*3)=109
109 % 10 = 9
So 15922-53-9 is a valid CAS Registry Number.

15922-53-9Downstream Products

15922-53-9Relevant academic research and scientific papers

CYCLOADDITION DES METHYLAZIDE ET PHENYLAZIDE AU β-NITROSTYRENE ET AU NITROPROPENE HOMOLOGUE

Cailleux, P.,Piet, J. C.,Benhaoua, H.,Carrie, R.

, p. 45 - 52 (2007/10/03)

Phenylazide and methylazide reacts with title olefines and gives two isomeric triazoles without nitro group, and 4-nitro-1,2,3 triazole.The isomerisation of starting alkenes explains the formation of isomeric triazoles.Oxydation of amino-nitro-diazocompounds in equilibrium with 1,2,3 triazolines leads to 4-nitro-1,2,3 triazoles.

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