113994-41-5 | 3-Ethyl 5-methyl 2-((2-aminoethoxy)methyl)-4-(2-chlorophenyl)-6-methylpyridine-3,5-dicarboxylate

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$965.00	$675.00

Description

• Catalog Number: AD36491
• Chemical Name: 3-Ethyl 5-methyl 2-((2-aminoethoxy)methyl)-4-(2-chlorophenyl)-6-methylpyridine-3,5-dicarboxylate
• CAS Number: 113994-41-5
• Molecular Formula: C20H23ClN2O5
• Molecular Weight: 406.86
• MDL Number: MFCD19705165
• SMILES: NCCOCc1nc(C)c(c(c1C(=O)OCC)c1ccccc1Cl)C(=O)OC

Upstream Synthesis Route

3-Ethyl 5-methyl 2-((2-aminoethoxy)methyl)-4-(2-chlorophenyl)-6-methylpyridine-3,5-dicarboxylate is a versatile compound that finds valuable applications in chemical synthesis. Thanks to its unique molecular structure, this compound serves as a crucial building block in the creation of advanced pharmaceuticals, agrochemicals, and specialty chemicals. Specifically, its presence of both carboxylate and amino moieties makes it a valuable intermediate in the synthesis of complex organic molecules.In chemical synthesis, 3-Ethyl 5-methyl 2-((2-aminoethoxy)methyl)-4-(2-chlorophenyl)-6-methylpyridine-3,5-dicarboxylate can be used to introduce functional groups or specific chemical motifs into target molecules. Its ability to undergo diverse chemical transformations, such as acylation, alkylation, or cross-coupling reactions, makes it a powerful tool for the construction of new chemical entities with desired properties. By strategically incorporating this compound into synthetic pathways, chemists can access novel compounds with enhanced biological activities or tailored functionalities.Additionally, the structural features of 3-Ethyl 5-methyl 2-((2-aminoethoxy)methyl)-4-(2-chlorophenyl)-6-methylpyridine-3,5-dicarboxylate make it a valuable scaffold for the development of molecular probes or drug candidates. Its unique combination of aromatic rings, heteroatoms, and flexible linkers offers opportunities for molecular diversification and structure-activity relationship studies. Through rational design and synthetic manipulation, researchers can exploit the chemical reactivity of this compound to create libraries of analogs for screening against biological targets or for structure-based drug design efforts.Overall, the versatility and synthetic utility of 3-Ethyl 5-methyl 2-((2-aminoethoxy)methyl)-4-(2-chlorophenyl)-6-methylpyridine-3,5-dicarboxylate establish it as a valuable tool in the arsenal of chemists working on the frontier of chemical synthesis and drug discovery.