111011-63-3 | 2-[benzyl(phenyl)amino]ethyl 5-(5,5-dimethyl-2-oxo-1,3,2$l^{5}-dioxaphosphinan-2-yl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
5mg	≥98%	in stock	$88.00	$62.00
10mg	≥98%	in stock	$134.00	$94.00
50mg	≥98%	in stock	$389.00	$272.00
100mg	≥98%	in stock	$688.00	$482.00

Description

• Catalog Number: AE11418
• Chemical Name: 2-[benzyl(phenyl)amino]ethyl 5-(5,5-dimethyl-2-oxo-1,3,2$l^{5}-dioxaphosphinan-2-yl)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate
• CAS Number: 111011-63-3
• Molecular Formula: C34H38N3O7P
• Molecular Weight: 631.6552
• MDL Number: MFCD00865899
• SMILES: CC1=C(C(=O)OCCN(c2ccccc2)Cc2ccccc2)C(C(=C(N1)C)P1(=O)OCC(CO1)(C)C)c1cccc(c1)[N+](=O)[O-]

Upstream Synthesis Route

3-Pyridinecarboxylic acid, 5-(5,5-dimethyl-2-oxido-1,3,2-dioxaphosphorinan-2-yl)-1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-, 2-[phenyl(phenylmethyl)amino]ethyl ester is a valuable compound in chemical synthesis due to its versatility in various reactions. This compound can serve as a key intermediate in the synthesis of complex organic molecules through its ability to undergo multiple chemical transformations.One application of this compound lies in its use as a building block for the synthesis of pharmaceutical intermediates. By functionalizing specific groups within the molecule, chemists can access a variety of structural motifs that are crucial for drug design and development. Additionally, the presence of the pyridine ring in the compound imparts unique chemical reactivity, allowing for further derivatization and diversification of the molecule.Furthermore, this compound can participate in transition metal-catalyzed reactions to introduce various functional groups, enabling the construction of intricate molecular architectures. Its structural features make it suitable for accessing challenging bond formations and stereochemistry, making it a valuable tool in the realm of chemical synthesis.