71172-77-5 Usage
Uses
Used in Pharmaceutical Industry:
2-(piperidin-1-ylMethyl)pyridine is used as a building block for the synthesis of various pharmaceutical products and drug molecules. Its structural characteristics make it a valuable component in the development of new medications.
Used in Research and Development:
In the realm of research and development, 2-(piperidin-1-ylMethyl)pyridine is utilized for the creation of new pharmaceutical compounds. Its unique properties allow scientists to explore its potential in formulating innovative drugs.
Used in Medicinal Chemistry:
2-(piperidin-1-ylMethyl)pyridine is also used as a subject of interest for further investigation in the field of medicinal chemistry. Studies on its biological and pharmacological activities aim to uncover its potential applications in treating various health conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 71172-77-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,1,7 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71172-77:
(7*7)+(6*1)+(5*1)+(4*7)+(3*2)+(2*7)+(1*7)=115
115 % 10 = 5
So 71172-77-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2/c1-4-8-13(9-5-1)10-11-6-2-3-7-12-11/h2-3,6-7H,1,4-5,8-10H2
71172-77-5Relevant academic research and scientific papers
Metal-Free Aminomethylation of Aromatic Sulfones Promoted by Eosin Y
Thierry, Thibault,Pfund, Emmanuel,Lequeux, Thierry
supporting information, p. 14826 - 14830 (2021/10/01)
A metal-free α-aminomethylation of heteroaryls promoted by eosin Y under green light irradiation is reported. A large variety of α-trimethylsilylamines as precursor of α-aminomethyl radical species were engaged to functionalize sulfonyl-heteroaryls following a Homolytic Aromatic Substitution (HAS) pathway. This method has provided a range of α-aminoheteroaryl compounds including a functionalized natural product. The mechanism of this late-stage functionalization of aryls was investigated and suggests the formation of a sulfonyl radical intermediate over a reductive quenching cycle.
