959246-63-0 Usage
Chemical class
Piperazine, a heterocyclic compound with a nitrogen-containing six-membered ring structure.
Molecular weight
304.33 g/mol, indicating the mass of one mole of the compound.
BOC protecting group
tert-butyloxycarbonyl group, which serves to protect the nitrogen atom in the piperazine ring during chemical reactions.
Functional groups
3-carboxymethyl-4-oxo-3,4-dihydroquinazolin-6-yl moiety, a complex functional group that contributes to the compound's biological activity.
Potential applications
Medicinal chemistry, specifically in the development of pharmaceutical drugs due to its ability to interact with various biological targets.
Versatility
The compound's structure and properties make it suitable for a wide range of drug development applications.
Organic synthesis utility
The presence of the BOC protecting group allows for selective manipulation of the piperazine moiety, making it useful in organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 959246-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,2,4 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 959246-63:
(8*9)+(7*5)+(6*9)+(5*2)+(4*4)+(3*6)+(2*6)+(1*3)=220
220 % 10 = 0
So 959246-63-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H24N4O5/c1-19(2,3)28-18(27)22-8-6-21(7-9-22)13-4-5-15-14(10-13)17(26)23(12-20-15)11-16(24)25/h4-5,10,12H,6-9,11H2,1-3H3,(H,24,25)
959246-63-0Relevant articles and documents
Non-peptide glycoprotein IIb/IIIa antagonists. 11. Design and in vivo evaluation of 3,4-dihydro-1(1H)-isoquinolinone-based antagonists and ethyl ester prodrugs
Hutchinson, John H.,Cook, Jacquelynn J.,Brashear, Karen M.,Breslin, Michael J.,Glass, Joan D.,Gould, Robert J.,Halczenko, Wasyl,Holahan, Marie A.,Lynch, Robert J.,Sitko, Gary R.,Stranieri, Maria T.,Hartman, George D.
, p. 4583 - 4591 (1996)
The structure-activity relationship of a series of orally active glycoprotein IIb/IIIa antagonists containing a nitrogen heterocycle grafted onto a 3,4-dihydro-1(1H)-isoquinolinone core is described. These compounds are structurally novel analogs of the p
