53422-71-2 Usage
Uses
Used in Organic Synthesis:
2-(3,4,5,6-tetrahydropyridin-2-yl)pyridine is utilized as a key intermediate in organic synthesis for the development of complex organic molecules. Its distinctive structure allows for versatile chemical reactions, making it a valuable component in the synthesis of various organic compounds.
Used in Chemical Research:
In the field of chemical research, 2-(3,4,5,6-tetrahydropyridin-2-yl)pyridine is employed as a model compound to study the properties and reactivity of heterocyclic systems. Its unique structure provides insights into the behavior of similar compounds and contributes to the advancement of chemical knowledge.
Used in Medicinal Chemistry and Pharmaceutical Research:
2-(3,4,5,6-tetrahydropyridin-2-yl)pyridine may have potential applications in medicinal chemistry and pharmaceutical research due to its distinctive molecular structure and properties. However, further studies and research are required to fully explore its potential uses and effects in these fields.
While the provided materials do not specify particular industries for the applications of 2-(3,4,5,6-tetrahydropyridin-2-yl)pyridine, the compound's uses are generally applicable across various sectors within the chemical, pharmaceutical, and research industries. Its role as a building block in organic synthesis and its potential in medicinal chemistry suggest that it could be relevant to industries such as pharmaceuticals, agrochemicals, and materials science, among others.
Check Digit Verification of cas no
The CAS Registry Mumber 53422-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,2 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 53422-71:
(7*5)+(6*3)+(5*4)+(4*2)+(3*2)+(2*7)+(1*1)=102
102 % 10 = 2
So 53422-71-2 is a valid CAS Registry Number.
53422-71-2Relevant academic research and scientific papers
Synthesis and kinetic resolution of N-Boc-2-arylpiperidines
Cochrane, Edward J.,Leonori, Daniele,Hassall, Lorraine A.,Coldham, Iain
supporting information, p. 9910 - 9913 (2014/08/18)
The chiral base n-BuLi/(-)-sparteine or n-BuLi/(+)-sparteine surrogate promotes kinetic resolution of N-Boc-2-arylpiperidines by asymmetric deprotonation. The enantioenriched starting material was recovered with yields 39-48% and ers up to 97:3. On lithiation then electrophilic quench, 2,2-disubstituted piperidines were obtained with excellent yields and enantioselectivities.
