57230-73-6

Basic information

• Product Name: 2-(4-acetylaminophenyl)-4,6-diamino-1,3,5-triazine
• Synonyms: 2-(4-acetylaminophenyl)-4,6-diamino-1,3,5-triazine
• CAS NO: 57230-73-6
• Molecular Weight: 259.271
• Mol File: 57230-73-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(4-acetylaminophenyl)-4,6-diamino-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-acetylaminophenyl)-4,6-diamino-1,3,5-triazine(57230-73-6)
• EPA Substance Registry System: 2-(4-acetylaminophenyl)-4,6-diamino-1,3,5-triazine(57230-73-6)

Safety Data

• Hazardous Substances Data: 57230-73-6(Hazardous Substances Data)

Upstream product

• 3397-62-4 2-Chloro-4,6-diamino-1,3,5-triazine 
• 122-80-5 N-acetyl-p-phenylenediamine 

Downstream Products

• 265103-45-5 N¹-4-[(4,6-diamino-1,3,5-triazin-2-yl)amino]phenyl-2-(acetylamino)-3-methyl-3-sulfanylbutanamide 
• 57230-74-7 2-(4-aminophenylamino)-4,6-diamino-1,3,5-triazine 

Relevant articles and documents

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

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.