1-(4-aminophenyl)piperidine-2,6-dione, also known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure and reactivity make it an essential building block in the creation of various pharmaceuticals, agrochemicals, and materials.In organic synthesis, $name$ serves as a key intermediate in the preparation of complex molecules due to its ability to undergo diverse chemical transformations. It can participate in various reactions such as acylation, alkylation, and condensation, leading to the formation of structurally intricate compounds. Additionally, the presence of the piperidine ring in $name$ imparts specific stereochemical properties, making it invaluable for the synthesis of chiral molecules with high enantioselectivity.Moreover, the amino and carbonyl groups present in $name$ offer multiple functionalization sites, allowing for the introduction of additional substituents to fine-tune the properties of the resulting products. This flexibility in derivatization is particularly advantageous in drug discovery and development, where small modifications in molecular structure can significantly impact biological activity and pharmacokinetic properties.Overall, the strategic incorporation of 1-(4-aminophenyl)piperidine-2,6-dione in chemical synthesis enables the efficient construction of diverse compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.
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