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• Solvents and Organic Chemicals Organic Compounds Alkaloids and derivatives Alkaloids and derivatives
• Solvents and Organic Chemicals Organic Compounds Alkaloids and derivatives

Compound CAS No. 34366-21-7: (R)-3-(Piperidin-2-YL)Pyridine

Compound CAS No. 34366-21-7, also known as (R)-3-(Piperidin-2-YL)Pyridine, is a structurally unique organic compound that has garnered significant attention in the fields of organic chemistry, pharmacology, and materials science. This compound is characterized by its pyridine ring fused with a piperidine moiety, which imparts it with distinctive electronic and steric properties. The (R)-configuration at the piperidine nitrogen further adds to its stereochemical complexity, making it a valuable substrate for asymmetric synthesis and enantioselective catalysis.

Recent advancements in synthetic methodology have enabled the efficient synthesis of (R)-3-(Piperidin-2-YL)Pyridine through various routes, including palladium-catalyzed cross-coupling reactions and organocatalytic processes. These methods have not only improved the yield and purity of the compound but also opened new avenues for its application in drug discovery. For instance, studies have shown that this compound exhibits potential as a lead molecule in the development of novel antipsychotic agents due to its ability to modulate dopamine receptor activity.

In addition to its pharmacological applications, (R)-3-(Piperidin-2-YL)Pyridine has also been explored in the realm of materials science. Its ability to form stable coordination complexes with transition metals has made it a promising candidate for use in catalysis and sensor technology. Recent research has demonstrated its utility as a chiral ligand in asymmetric hydrogenation reactions, where it has shown exceptional enantioselectivity and turnover numbers.

The stereochemical properties of (R)-3-(Piperidin-2-YL)Pyridine have also been leveraged in the design of chiral recognition systems. By incorporating this compound into self-assembled monolayers, researchers have developed surfaces with high enantioselectivity, which could find applications in enantiomeric resolution and chiral sensing.

Moreover, the electronic properties of (R)-3-(Piperidin-2-YL)Pyridine make it an attractive candidate for use in organic electronics. Its ability to act as an electron-deficient aromatic system has been exploited in the design of novel π-conjugated materials for use in organic photovoltaics and light-emitting diodes (OLEDs). Recent studies have highlighted its potential as a building block for constructing low-bandgap semiconductors with high charge carrier mobility.

In terms of biological activity, (R)-3-(Piperidin-2-YL)Pyridine has been shown to exhibit moderate inhibitory effects on several enzymes, including kinases and proteases. This suggests that it could serve as a starting point for developing small-molecule inhibitors targeting these enzymes. Furthermore, its ability to penetrate cellular membranes makes it a potential candidate for drug delivery systems.

From a synthetic standpoint, the preparation of (R)-3-(Piperidin-2-YL)Pyridine involves a series of carefully optimized steps to ensure high enantiomeric purity. The use of chiral auxiliaries and asymmetric induction techniques has been instrumental in achieving this goal. Recent advancements in flow chemistry have further enhanced the scalability and reproducibility of these synthetic protocols.

In conclusion, Compound CAS No. 34366-21-7: (R)-3-(Piperidin-2-YL)Pyridine is a versatile compound with a wide range of applications across multiple disciplines. Its unique structure, stereochemical properties, and electronic characteristics make it an invaluable tool for researchers in academia and industry alike. As ongoing research continues to uncover new facets of its potential, this compound is poised to play an increasingly important role in the development of novel materials and therapeutic agents.

• 494-52-0(Anabasine)
• 13078-04-1(3-(Piperidin-2-yl)pyridine)
• 62784-11-6(Pyridine, 3-(1-hexyl-2-piperidinyl)-, (S)-)
• 130342-99-3(2-(Pyridin-3-yl)azepane)
• 2055-12-1(N-Methyl Anabasine)
• 18793-19-6(Pyridine,3-[(2R,4S)-2-(3-pyridinyl)-4-piperidinyl]-, rel-)
• 24380-92-5(N-Methyl anabasine)
• 15251-47-5(Anabasine Hydrochloride)
• 53912-89-3((+)-Anabasine Hydrochloride)
• 62784-04-7(Pyridine, 3-(1-pentyl-2-piperidinyl)-, (S)- (9CI))