124886-01-7 Usage
Class
Hetrocyclic compounds
Heteroatom
Nitrogen
Type
Synthetic organic compound
Natural Occurrence
Not commonly found in nature
Structural Similarity
To certain biologically active compounds
Potential Applications
Pharmaceutical industry (requires further research)
Biological Properties
Not widely documented (requires further research)
Chemical Properties
Not widely documented (requires further research)
Research Status
Further research and investigation needed for exact properties and potential uses
Check Digit Verification of cas no
The CAS Registry Mumber 124886-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,8,8 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124886-01:
(8*1)+(7*2)+(6*4)+(5*8)+(4*8)+(3*6)+(2*0)+(1*1)=137
137 % 10 = 7
So 124886-01-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H11N3O/c1-6-3-4-9-8(7(6)2)5-10-11(13-9)15-12(16)14-10/h3-5H,1-2H3,(H2,13,14,15,16)
124886-01-7Relevant academic research and scientific papers
1,3-dihydro-2H-imidazo[4,5-b]quinolin-2-ones - Inhibitors of blood platelet cAMP phosphodiesterase and induced aggregation
Meanwell,Roth,Smith,Wedding,Wright,Fleming,Gillespie
, p. 2906 - 2916 (2007/10/02)
A series of 1,3-dihydro-2H-imidazo[4,5-b]quinolin-2-one derivatives was synthesized and evaluated as inhibitors of cAMP hydrolysis by a crude human platelet phosphodiesterase preparation and as inhibitors of ADP- and collagen-induced aggregation of rabbit
Imidazoquinoline antithrombrogenic cardiotonic agents
-
, (2008/06/13)
Novel series of 1,3-dihydro-2H-imidazo[4,5-b]quinolin-2-ones of the Formula STR1 wherein R1 is halogen, lower alkyl, lower alkoxy, trifluoromethyl; R2 is hydrogen, halogen, lower alkyl, lower alkoxy; R3 is hydrogen, haloge
