87597-20-4 Usage
Uses
Used in Pharmaceutical Industry:
IMIDAZO[1,2-A]PYRAZINE-8-CARBOXYLIC ACID ETHYL ESTER is used as a key intermediate for the synthesis of various pharmaceuticals and biologically active molecules. Its unique structure and properties allow it to be a crucial component in the creation of new drugs and therapeutic agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, IMIDAZO[1,2-A]PYRAZINE-8-CARBOXYLIC ACID ETHYL ESTER is used as a building block for designing and developing novel drug candidates. Its potential in treating various diseases and disorders makes it an important compound in the pursuit of medical advancements.
Used in Drug Development:
IMIDAZO[1,2-A]PYRAZINE-8-CARBOXYLIC ACID ETHYL ESTER is utilized as a starting material in drug development processes. Its chemical versatility enables the creation of a wide range of drug candidates with different therapeutic targets and mechanisms of action.
Used in the Synthesis of Biologically Active Molecules:
IMIDAZO[1,2-A]PYRAZINE-8-CARBOXYLIC ACID ETHYL ESTER is also used in the synthesis of biologically active molecules, which can have significant applications in medicine and healthcare. Its unique structure allows for the development of molecules with specific biological activities, contributing to the discovery of new treatments and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 87597-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,9 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87597-20:
(7*8)+(6*7)+(5*5)+(4*9)+(3*7)+(2*2)+(1*0)=184
184 % 10 = 4
So 87597-20-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H9N3O2/c1-2-14-9(13)7-8-11-4-6-12(8)5-3-10-7/h3-6H,2H2,1H3
87597-20-4Relevant academic research and scientific papers
Synthesis of imidazo[1,2-a]pyrazine derivatives with uterine-relaxing, antibronchospastic, and cardiac-stimulating properties
Sablayrolles,Cros,Milhavet,Rechenq,Chapat,Boucard,Serrano,McNeill
, p. 206 - 212 (2007/10/02)
A series of imidazo[1,2-a]pyrazine derivatives was synthesized by condensation of α-halogenocarbonyl compounds and aminopyrazines. Various compounds resulted from competitive reactions or reagent isomerization and demonstrated in vitro uterine-relaxing and in vivo antibronchospastic activities. On isolated atria, 5-bromoimidazo[1,2-a]pyrazine showed positive chronotropic and inotropic properties; the latter was associated with an increase in the cyclic AMP tissue concentration. Potentiation of the isoproterenol positive inotropic effect of 5-bromoimidazo[1,2-a]pyrazine and the lack of blockade of the 5-bromoimidazo[1,2-a]pyrazine positive inotropic effect by propranolol suggested phosphodiesterase-inhibiting properties.
