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2-PIPERIDYLMETHYLAMINE CAS:22990-77-8

2-Piperidylmethylamine is an organic compound featuring a piperidine ring with a methylamine group attached to the 2-position. This structure grants it unique chemical properties and potential biological activities. As a derivative of piperidine, it can interact with various receptors and enzymes in biological systems, suggesting possible applications in medicinal chemistry. Due to its amine functionality, 2-piperidylmethylamine may participate in hydrogen bonding, influencing its solubility and binding affinity for target molecules. Its exploration could lead to discoveries in drug development, particularly in fields related to neuropharmacology and the treatment of psychiatric disorders.


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Application and Effect:

2-Piperidylmethylamine is an intriguing compound that combines the structural features of a piperidine ring with a methylamine side chain. The molecular framework consists of a six-membered nitrogen-containing heterocycle (piperidine) at the core, which is known for its presence in numerous biologically active compounds. The addition of a methylamine group at the 2-position enhances the molecule's potential reactivity and biological interactions. The piperidine moiety contributes to the overall stability of the compound, while the amine functionality introduces basicity, allowing for protonation under physiological conditions. This property makes 2-piperidylmethylamine a suitable candidate for engaging with various biological targets, including neurotransmitter receptors and enzymes involved in neurotransmission. As such, it may exhibit pharmacological properties that can be harnessed in the development of therapeutics for conditions such as depression, anxiety, or neurological disorders. Research has shown that piperidine derivatives can modulate neurotransmitter systems, particularly those involving serotonin, dopamine, and norepinephrine. Given its structural characteristics, 2-piperidylmethylamine could serve as a scaffold for the synthesis of novel compounds aimed at enhancing these interactions. Furthermore, modifications to the piperidine ring or the amine substituent could lead to derivatives with improved potency or selectivity for specific targets. In addition to its medicinal implications, 2-piperidylmethylamine may find applications in synthetic organic chemistry as a building block in the design of ligands and catalysts. Its ability to form stable complexes with metal ions also suggests utility in coordination chemistry. In conclusion, 2-piperidylmethylamine presents a valuable framework for research across multiple disciplines, from drug discovery to material science. Ongoing investigations into its biological activity and synthetic versatility hold promise for unlocking new therapeutic strategies and advancing knowledge in organic synthesis.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C6H14N2
Assay 99%
Appearance white powder
CAS No.  22990-77-8
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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