51132-01-5 Usage
Heterocyclic compound
The compound contains atoms of different elements (heteroatoms) in its ring structure, such as nitrogen and oxygen, in addition to carbon atoms.
Fused imidazo-pyridine ring system
The compound has a complex structure with a fused ring system that includes both imidazo and pyridine rings.
Key component in drug development
The chemical structure of 2-[2-(imidazo[1,2-a]pyridin-2-yl)ethyl]-1H-isoindole-1,3(2H)-dione is important in the creation of new drugs and pharmaceuticals due to its unique properties.
Potential for biological activity
2-[2-(imidazo[1,2-a]pyridin-2-yl)ethyl]-1H-isoindole-1,3(2H)-dione has the possibility of exhibiting biological activities, making it a potential candidate for medicinal chemistry research.
Synthesis of new organic compounds
The compound can be used as a building block for creating new organic compounds with a variety of pharmacological properties.
Diverse pharmacological properties
The potential applications of 2-[2-(imidazo[1,2-a]pyridin-2-yl)ethyl]-1H-isoindole-1,3(2H)-dione may include a range of therapeutic effects and medicinal uses.
Need for further research
More investigation is required to fully explore the potential applications of 2-[2-(imidazo[1,2-a]pyridin-2-yl)ethyl]-1H-isoindole-1,3(2H)-dione in medicine and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 51132-01-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,3 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51132-01:
(7*5)+(6*1)+(5*1)+(4*3)+(3*2)+(2*0)+(1*1)=65
65 % 10 = 5
So 51132-01-5 is a valid CAS Registry Number.
51132-01-5Relevant academic research and scientific papers
Gold-catalyzed redox synthesis of imidazo[1,2-a]pyridines using pyridine N-oxide and alkynes
Talbot, Eric P. A.,Richardson, Melodie,McKenna, Jeffrey M.,Toste, F. Dean
supporting information, p. 687 - 691 (2014/04/03)
A mild, catalytic, atom economical synthesis of imidazo[1,2-a]pyridines has been developed: catalytic dichloro(2-pyridinecarboxylato)gold [PicAuCl 2] in the presence of an acid produces a range of imidazo[1,2-a]pyridines in good yields starting
IMIDAZO[1,2-a]PYRIDINES
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, (2008/06/13)
The compounds are imidazo 1,2-a!pyridines which possess activity similar to histamine, in particular, they are agonists of H-1 histamine receptors. A compound of this invention is 2-(2-aminoethyl) imidazo 1,2-a!pyridine.
