2,4-Piperidinedione, 6-methyl-, (6S)-


Chemical Name: 2,4-Piperidinedione, 6-methyl-, (6S)-
CAS Number: 653589-26-5
Product Number: AG006SDG(AGN-PC-0OF7PL)
Synonyms:
MDL No:
Molecular Formula: C6H9NO2
Molecular Weight: 127.1412

Identification/Properties


Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



(S)-6-Methylpiperidine-2,4-dione, also known as N-Formylpiperidine or N-Formyl-6-methylpiperidin-2,4-dione, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals.One of the primary applications of (S)-6-Methylpiperidine-2,4-dione is in the production of piperidine derivatives, which are essential building blocks in the pharmaceutical industry. By incorporating this compound into the synthesis route, chemists can access a diverse range of pharmacologically active compounds with piperidine moieties. These derivatives exhibit a wide spectrum of biological activities and are utilized in the development of drugs for various therapeutic areas.Furthermore, (S)-6-Methylpiperidine-2,4-dione can serve as a valuable starting material for the preparation of heterocyclic compounds. Its unique structural features enable the introduction of functional groups at specific positions, allowing for the synthesis of complex molecules with desired properties. This compound's reactivity and versatility make it a valuable tool in the hands of synthetic chemists for the efficient construction of diverse chemical structures.Overall, the strategic utilization of (S)-6-Methylpiperidine-2,4-dione in chemical synthesis enables the synthesis of structurally diverse compounds with potential applications in pharmaceuticals, agrochemicals, and materials science. Its role as a key intermediate highlights its importance in the synthesis of complex molecules with tailored properties and biological activities.