85102-27-8 Usage
Description
Imidazo[1,2-a]pyridine, 7-phenylis a chemical compound with the molecular formula C13H9N. It is a derivative of imidazopyridine and contains a phenyl group at the seventh position. Imidazo[1,2-a]pyridine, 7-phenylis known for its potential pharmaceutical and biological applications, particularly in the field of medicinal chemistry. Imidazo[1,2-a]pyridine, 7-phenylhas been studied for its potential as a drug candidate for various therapeutic indications, including antiviral, antibacterial, and anticancer activities. It is of interest to researchers and chemists seeking to explore its potential as a novel pharmaceutical agent.
Uses
Used in Pharmaceutical Industry:
Imidazo[1,2-a]pyridine, 7-phenylis used as a drug candidate for its potential antiviral, antibacterial, and anticancer activities. Its unique structure and properties make it a promising candidate for the development of new therapeutic agents.
Used in Medicinal Chemistry Research:
Imidazo[1,2-a]pyridine, 7-phenylis used as a subject of study in medicinal chemistry research to explore its potential applications and mechanisms of action. This can lead to the discovery of new drugs and therapies for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 85102-27-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,0 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85102-27:
(7*8)+(6*5)+(5*1)+(4*0)+(3*2)+(2*2)+(1*7)=108
108 % 10 = 8
So 85102-27-8 is a valid CAS Registry Number.
85102-27-8Relevant articles and documents
Pd-Catalyzed Tandem Cyclization via C-H Arylation and Acylation for the Construction of Polycyclic Scaffolds
Mu, Bing,Li, Jingya,Zou, Dapeng,Wu, Yusheng,Chang, Junbiao,Wu, Yangjie
supporting information, p. 5260 - 5263 (2016/11/02)
The first Pd-catalyzed tandem cyclization of imidazo[1,2-a]pyridines with 2-chlorobenzaldehydes through C-H arylation and acylation is presented for the efficient synthesis of novel 6H-benzo[b]imidazo[5,1,2-de]quinolizin-6-ones. The direct acylation react
Design and synthesis of 3,7-diarylimidazopyridines as inhibitors of the VEGF-receptor KDR
Wu, Zhicai,Fraley, Mark E.,Bilodeau, Mark T.,Kaufman, Mildred L.,Tasber, Edward S.,Balitza, Adrienne E.,Hartman, George D.,Coll, Kathleen E.,Rickert, Keith,Shipman, Jennifer,Shi, Bin,Sepp-Lorenzino, Laura,Thomas, Kenneth A.
, p. 909 - 912 (2007/10/03)
3,7-Diarylsubstituted imidazopyridines were designed and developed as a new class of KDR kinase inhibitors. A variety of imidazopyridines were synthesized and potent inhibitors of KDR kinase activity were identified with good aqueous solubility.