22766-68-3 | Ethyl quinuclidine-4-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$18.00	$12.00
1g	98%	in stock	$21.00	$15.00
5g	98%	in stock	$104.00	$73.00
10g	98%	in stock	$207.00	$145.00
25g	98%	in stock	$418.00	$293.00

Description

• Catalog Number: AF32476
• Chemical Name: Ethyl quinuclidine-4-carboxylate
• CAS Number: 22766-68-3
• Molecular Formula: C10H17NO2
• Molecular Weight: 183.2475
• MDL Number: MFCD19686937
• SMILES: CCOC(=O)C12CCN(CC1)CC2

Upstream Synthesis Route

Ethyl quinuclidine-4-carboxylate, also known as EQC, is a versatile chemical compound widely used in organic synthesis due to its unique structural properties. This compound serves as a key building block in the preparation of various complex molecules and pharmaceuticals.One of the prominent applications of Ethyl quinuclidine-4-carboxylate in chemical synthesis is its role as a precursor in the synthesis of heterocyclic compounds. By undergoing specific chemical reactions, EQC can be transformed into various functionalized quinuclidine derivatives, which are essential intermediates in the synthesis of pharmaceuticals, agrochemicals, and other bioactive compounds.Additionally, Ethyl quinuclidine-4-carboxylate can participate in cycloaddition reactions, enabling the formation of fused ring systems with multiple functionalities. This property makes EQC a valuable tool in the design and synthesis of complex molecular structures with diverse applications in medicinal chemistry and material science.Moreover, EQC can be utilized in asymmetric synthesis to introduce chirality into the final products. By employing chiral catalysts or reagents, Ethyl quinuclidine-4-carboxylate can facilitate the creation of enantiomerically pure compounds, which are crucial in drug development and other industries requiring optically active molecules.Overall, the versatile nature of Ethyl quinuclidine-4-carboxylate makes it a valuable reagent in chemical synthesis, enabling the construction of diverse molecular architectures with precise control over stereochemistry and functionality.