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[1,2,4]Triazolo[1,5-a][1,3,5]triazine-5,7-diamine, N,N,N',N'-tetramethyl-2-phenyl- is a complex organic compound with the molecular formula C13H16N6. It features a triazolo-triazine ring system, which is a fused ring structure consisting of a triazole and a triazine. The compound is characterized by two amine groups at the 5 and 7 positions, and a phenyl group attached to the 2 position. The N,N,N',N'-tetramethyl substitution refers to four methyl groups attached to the nitrogen atoms, which can influence the compound's physical and chemical properties, such as solubility and reactivity. This specific structure may be of interest in various chemical and pharmaceutical applications due to its unique electronic and steric properties.

54807-00-0

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54807-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54807-00-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,0 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54807-00:
(7*5)+(6*4)+(5*8)+(4*0)+(3*7)+(2*0)+(1*0)=120
120 % 10 = 0
So 54807-00-0 is a valid CAS Registry Number.

54807-00-0Downstream Products

54807-00-0Relevant academic research and scientific papers

Triazines and Related Products. Part 26. Synthesis and Chemistry of Bicyclic Analogues of the Antitumour Drug 2,4,6-Tris(dimethylamino)-1,3,5-triazine (Hexamethylmelamine)

Langdon, Simon P.,Simmonds, Richard J.,Stevens, Malcolm F. G.

, p. 993 - 998 (2007/10/02)

Interaction of 2,4-bis(dimethylamino)-6-hydrazino-1,3,5-triazine (1c) with aryl aldehydes yields a series of aryl hydrazones (4) which cyclise to 3-aryl-5,7-bis(dimethylamino)-1,2,4-triazolotriazines (6) with lead(VI) acetate in dichloromethane.Rearrangement of these bicycles in methanolic sodium hydroxide affords stable isomeric 2-aryl-5,7-bis(dimethylamino)triazolotriazines (7).Selected examples from both series of triazolotriazines were screened against the mouse M5076 reticulum cell sarcoma and P388 leukaemia in vivo but proved to have no antitumour activity.

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