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AI05006

100710-37-0 | 2-(2-Naphthyl)pyrrolidine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $169.00 $118.00 -   +
250mg 95% in stock $265.00 $186.00 -   +
1g 95% in stock $634.00 $444.00 -   +
5g 95% in stock $1,878.00 $1,315.00 -   +
10g 95% in stock $2,810.00 $1,967.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AI05006
Chemical Name: 2-(2-Naphthyl)pyrrolidine
CAS Number: 100710-37-0
Molecular Formula: C14H15N
Molecular Weight: 197.2756
MDL Number: MFCD02663521
SMILES: C1CNC(C1)c1ccc2c(c1)cccc2

 

Upstream Synthesis Route
  • Known for its versatile applications in chemical synthesis, 2-(2-Naphthalenyl)pyrrolidine is a valuable compound that serves as a key building block in the preparation of various organic molecules. Its unique structure, characterized by the presence of a pyrrolidine ring attached to a naphthalene moiety, imparts distinct properties that are exploited in a range of synthetic processes.One of the primary uses of 2-(2-Naphthalenyl)pyrrolidine is as a chiral auxiliary in asymmetric synthesis. By utilizing this compound, chemists can introduce chirality into molecules in a controlled manner, facilitating the production of enantiomerically pure compounds with high optical purity. This application is particularly crucial in the pharmaceutical industry, where the biological activity of drugs often depends on the stereochemistry of the molecules.Another significant role of 2-(2-Naphthalenyl)pyrrolidine in chemical synthesis is its function as a ligand in transition metal catalyzed reactions. The presence of the naphthalene group enables the compound to coordinate with metal ions, promoting catalytic reactions that are essential for the construction of complex organic frameworks. This catalytic activity has been instrumental in the development of efficient and sustainable synthetic methodologies that are employed in the production of fine chemicals and pharmaceutical intermediates.Overall, the strategic incorporation of 2-(2-Naphthalenyl)pyrrolidine into synthetic pathways showcases its utility as a multifaceted reagent that enhances the efficiency and selectivity of chemical transformations. Whether employed as a chiral template for asymmetric synthesis or as a ligand in catalytic processes, this compound continues to play a crucial role in advancing the frontiers of modern organic chemistry.
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