117719-10-5 Usage
General Description
2-AMINO-5-BROMO-3-(ETHYLAMINO)PYRAZINE is a chemical compound with the molecular formula C6H8BrN5. It is a pyrazine derivative consisting of a 2-amino-5-bromo-3-(ethylamino)pyrazine core, which is commonly used in the synthesis of pharmaceuticals and agrochemicals. 2-AMINO-5-BROMO-3-(ETHYLAMINO)PYRAZINE is known for its potential as a building block in organic synthesis, and it has shown various biological activities, including as an antifungal and antibacterial agent. Additionally, it has been studied for its potential in the treatment of neurological disorders and cancer. Due to its versatile properties and potential applications, 2-AMINO-5-BROMO-3-(ETHYLAMINO)PYRAZINE is a valuable compound in the field of medicinal chemistry and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 117719-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,7,1 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 117719-10:
(8*1)+(7*1)+(6*7)+(5*7)+(4*1)+(3*9)+(2*1)+(1*0)=125
125 % 10 = 5
So 117719-10-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H9BrN4/c1-2-9-6-5(8)10-3-4(7)11-6/h3H,2H2,1H3,(H2,8,10)(H,9,11)
117719-10-5Relevant articles and documents
New imidazo[1,2-a]pyrazine derivatives with bronchodilatory and cyclic nucleotide phosphodiesterase inhibitory activities
Vitse, Olivier,Laurent, Florence,Pocock, Tristan M.,Benezech, Veronique,Zanik, Lahcen,Elliott, Keith R. F.,Subra, Guy,Portet, Karine,Bompart, Jacques,Chapat, Jean-Pierre,Small, Roger C.,Michel, Alain,Bonnet, Pierre-Antoine
, p. 1059 - 1065 (2007/10/03)
New imidazo[1,2-a]pyrazine derivatives have been synthesized either by direct cyclization from pyrazines or by electrophilic substitutions. The presence of electron donating groups on position 8 greatly enhances the reactivity of the heterocycle towards such reactions on position 3 of the heterocycle. The activities of these derivatives in trachealis muscle relaxation and in inhibiting cyclic nucleotide phosphodiesterase (PDE) isoenzyme types III and IV have been assessed. All compounds demonstrated significantly higher relaxant potency than theophylline. All the derivatives were moderately potent in inhibiting the type IV isoenzyme of PDE but only those with a cyano group on position 2 were potent in inhibiting the type III isoenzyme. Copyright (C) 1999 Elsevier Science Ltd.
