53687-87-9 Usage
Uses
Used in Pharmaceutical Applications:
[2-(methylsulfanyl)imidazo[1,2-a]pyridin-3-yl](phenyl)methanone is used as a potential pharmaceutical compound for its unique molecular structure and the presence of the imidazopyridinyl group, which is commonly found in many drugs. [2-(methylsulfanyl)imidazo[1,2-a]pyridin-3-yl](phenyl)methanone's potential applications in medicinal chemistry are attributed to its aromatic and hydrophobic properties, as well as the sulfhydryl moiety introduced by the methylsulfanyl group.
Used in Medicinal Chemistry Research:
[2-(methylsulfanyl)imidazo[1,2-a]pyridin-3-yl](phenyl)methanone is used as a subject of study in medicinal chemistry research to understand its properties, reactivity, and potential applications. [2-(methylsulfanyl)imidazo[1,2-a]pyridin-3-yl](phenyl)methanone's unique molecular structure and the presence of the phenyl and imidazopyridinyl groups make it an interesting candidate for further analysis and development in the field of drug discovery and design.
Used in Drug Design and Development:
[2-(methylsulfanyl)imidazo[1,2-a]pyridin-3-yl](phenyl)methanone is used as a starting point or building block in drug design and development due to its unique molecular structure and potential pharmaceutical applications. [2-(methylsulfanyl)imidazo[1,2-a]pyridin-3-yl](phenyl)methanone's properties, such as its aromatic and hydrophobic characteristics, as well as the presence of the sulfhydryl moiety, make it a promising candidate for the development of new drugs with specific therapeutic targets.
Check Digit Verification of cas no
The CAS Registry Mumber 53687-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,8 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53687-87:
(7*5)+(6*3)+(5*6)+(4*8)+(3*7)+(2*8)+(1*7)=159
159 % 10 = 9
So 53687-87-9 is a valid CAS Registry Number.
53687-87-9Relevant academic research and scientific papers
Novel one-pot three component reaction for the synthesis of [2-(alkylsulfanyl)imidazo[1,2-a]pyridin-3-yl](aryl)methanone
Kianmehr, Ebrahim,Ghanbari, Mohammad,Niri, Mehri Nadiri,Faramarzi, Reza
experimental part, p. 41 - 44 (2010/10/03)
A one-pot, three-component reaction between pyridine, phenacyl bromide, and thiocyanate is described. The reaction afforded the corresponding special type of fully substituted imidazo[1,2-a]pyridine derivatives in good yields without using any catalyst or activation.
Reactions of Pyridinium or Isoquinolinium Ketene Dithioacetals with Aromatic N-Imines and S-Imines
Tominaga, Yoshinori,Hosomi, Akira
, p. 1449 - 1454 (2007/10/02)
Reactions of ketene dithioacetals, 1-pyridinium 1a-i or -isoquinolinium 2a,b iodides with aromatic N-imines, 1-aminopyridinium 3a-l, 1-aminoquinolinium (4), and 2-aminoisoquinolinium (5) mesitylene sulfonates gave the corresponding 2-methylthioimidazopyridines 9a-k, 2-methylthiopyrazolopyridines 11a-q, 2-methylthioimidazoisoquinoline derivatives 10a,b and 2-methylthiopyrazoloquinoline (12).The benzoyl compounds, 1-pyridinium iodides 1g,h,i reacted with N-imine 3a to give the 3-benzoyl-2-methylthioimidazopyridines 9h-k.The reaction of pyridinium ketene dithioacetals 1a,f,g (R1 = COOEt, COPh, and CN) with substituted pyridinium N-imines having an electron-withdrawing group on the pyridine ring afforded only the corresponding pyrazolopyridine derivatives 11j-r in good yields.Reactions of ketene dithioacetals with various S-imines are also described.Possible mechanisms for the formation of 9 and 11 are described.
