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2-(4-aminophenylamino)-4,6-diamino-1,3,5-triazine is a complex organic compound with the molecular formula C9H11N7. It is a derivative of 1,3,5-triazine, a heterocyclic compound consisting of three nitrogen atoms and three carbon atoms in a ring structure. The compound features two amino groups attached to the 4 and 6 positions of the triazine ring, and a 4-aminophenyl group attached to the 2 position. This structure endows the compound with various chemical properties and potential applications in fields such as pharmaceuticals, dyes, and materials science. Due to its multiple amino groups, it can participate in various chemical reactions, including condensation, substitution, and addition reactions, making it a versatile building block for the synthesis of more complex molecules.

57230-74-7

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57230-74-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57230-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,3 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57230-74:
(7*5)+(6*7)+(5*2)+(4*3)+(3*0)+(2*7)+(1*4)=117
117 % 10 = 7
So 57230-74-7 is a valid CAS Registry Number.

57230-74-7Relevant academic research and scientific papers

Synthesis, electrochemical, and spectroscopic studies of novel S-nitrosothiols

Soulère, Laurent,Sturm, Juan-Carlos,Nú?ez-Vergara, Luis J.,Hoffmann, Pascal,Périé, Jacques

, p. 7173 - 7180 (2007/10/03)

A series of S-nitrosothiol compounds, structurally related to the NO-donor S-nitroso-N-acetyl-D,L-penicillamine (SNAP) that contain amidin groups were synthesised by S-nitrosation of the corresponding thiols and characterised. The kinetics of decomposition were investigated and showed that the two adenine-based thionitrites exhibited an unusual stability in aqueous solution compared to SNAP, suggesting that these compounds may complex the traces of free copper ions present in solution, which is known to catalyze the decomposition of thionitrites. The electrochemical behaviour of these compounds and their nitric oxide-releasing potential were studied by means of cyclic voltammetry techniques on mercury and glassy carbon electrodes.

Synthesis and uptake of nitric oxide-releasing drugs by the P2 nucleoside transporter in trypanosoma equiperdum

Soulere, Laurent,Hoffmann, Pascal,Bringaud, Frederic,Perie, Jacques

, p. 1347 - 1350 (2007/10/03)

A series of S-nitrosothiols, structurally related to the NO-donor S-nitroso-N-acetylpenicillamine, and of organic nitrate esters that contain amidine groups which specify a recognition via the trypanosomal purine transporter P2, were synthesized and tested for their ability to inhibit the uptake of [2-3H]adenosine on Trypanosoma equiperdum. (C) 2000 Elsevier Science Ltd. All rights reserved.

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