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(4-Methyl-6-phenyl-pyridazin-3-yl)-(6-phenyl-pyridazin-3-yl)-amine is a complex organic compound characterized by its unique molecular structure. It features two pyridazine rings, each with a phenyl group attached to the 6th position. The first pyridazine ring also has a methyl group at the 4th position, while the second pyridazine ring is connected to the first through an amine group. (4-Methyl-6-phenyl-pyridazin-3-yl)-(6-phenyl-pyridazin-3-yl)-amine is known for its potential applications in the pharmaceutical industry, particularly in the development of drugs targeting various biological pathways. Its chemical properties and reactivity are influenced by the presence of the phenyl groups, which contribute to its stability and potential for further chemical modifications. The compound's structure and functional groups make it a subject of interest for researchers exploring new therapeutic agents and chemical intermediates.

81819-94-5

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81819-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81819-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,1 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81819-94:
(7*8)+(6*1)+(5*8)+(4*1)+(3*9)+(2*9)+(1*4)=155
155 % 10 = 5
So 81819-94-5 is a valid CAS Registry Number.

81819-94-5Downstream Products

81819-94-5Relevant academic research and scientific papers

Reactions of 3-Chloropyridazines with Some Nucleophilic Reagents

Moustafa, A. H.,Kaddah, A. M.,Shams, N. A.

, p. 1084 - 1086 (2007/10/02)

3-Chloro-6-phenylpyridazine (1a) and its 4-methyl derivative (1b) react with sodamide, hydrazines, 3-aminopyridazines and phenothiazine in polar and non-polar solvents as well as by fusion to give different products.The structures assigned to the products have been confirmed by their IR spectra.

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