Cas no 83413-42-7 (3-PIPERIDINONE, 6-METHYL-1-(PHENYLMETHYL)-)

3-Piperidinone, 6-methyl-1-(phenylmethyl)-, is a heterocyclic organic compound featuring a piperidinone core substituted with a methyl group at the 6-position and a benzyl group at the 1-position. This structure imparts versatility in synthetic applications, particularly in pharmaceutical and agrochemical research, where it serves as a key intermediate for the development of bioactive molecules. Its rigid framework and functional groups allow for selective modifications, enabling the synthesis of derivatives with tailored properties. The compound’s stability and well-defined reactivity profile make it suitable for use in controlled reactions, including alkylations, acylations, and nucleophilic substitutions, supporting efficient scaffold diversification in medicinal chemistry.
3-PIPERIDINONE, 6-METHYL-1-(PHENYLMETHYL)- structure
83413-42-7 structure
Product Name:3-PIPERIDINONE, 6-METHYL-1-(PHENYLMETHYL)-
CAS No:83413-42-7
MF:C13H17NO
MW:203.280183553696
CID:3297849
PubChem ID:434564
Update Time:2025-06-08

3-PIPERIDINONE, 6-METHYL-1-(PHENYLMETHYL)- Chemical and Physical Properties

Names and Identifiers

    • 3-PIPERIDINONE, 6-METHYL-1-(PHENYLMETHYL)-
    • 1-benzyl-6-methylpiperidin-3-one
    • AKOS026727548
    • 83413-42-7
    • 859-633-3
    • SCHEMBL15648976
    • EN300-78906
    • IDA41342
    • NSC352086
    • D85990
    • NSC-352086
    • Inchi: 1S/C13H17NO/c1-11-7-8-13(15)10-14(11)9-12-5-3-2-4-6-12/h2-6,11H,7-10H2,1H3
    • InChI Key: KZOQTVBEJPFESD-UHFFFAOYSA-N
    • SMILES: O=C1CCC(C)N(CC2C=CC=CC=2)C1

Computed Properties

  • Exact Mass: 203.131014166g/mol
  • Monoisotopic Mass: 203.131014166g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 2
  • Complexity: 221
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.1
  • Topological Polar Surface Area: 20.3?2

3-PIPERIDINONE, 6-METHYL-1-(PHENYLMETHYL)- Pricemore >>

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3-PIPERIDINONE, 6-METHYL-1-(PHENYLMETHYL)- Related Literature

Additional information on 3-PIPERIDINONE, 6-METHYL-1-(PHENYLMETHYL)-

Comprehensive Analysis of 3-PIPERIDINONE, 6-METHYL-1-(PHENYLMETHYL)- (CAS No. 83413-42-7)

The compound 3-PIPERIDINONE, 6-METHYL-1-(PHENYLMETHYL)- (CAS No. 83413-42-7) is a significant intermediate in organic synthesis and pharmaceutical research. Its unique structure, featuring a piperidinone core with a methyl group at the 6-position and a benzyl substitution at the 1-position, makes it a versatile building block for various applications. Researchers and industries are increasingly interested in this compound due to its potential in drug discovery, agrochemical development, and material science.

One of the most searched questions about 3-PIPERIDINONE, 6-METHYL-1-(PHENYLMETHYL)- revolves around its synthesis and purification methods. Recent advancements in green chemistry have led to more efficient and environmentally friendly protocols for producing this compound. For instance, catalytic hydrogenation and microwave-assisted synthesis are now widely adopted to improve yield and reduce waste. These methods align with the growing demand for sustainable chemical processes, a hot topic in both academic and industrial circles.

Another area of interest is the pharmacological properties of 3-PIPERIDINONE derivatives. Studies suggest that modifications to the piperidinone scaffold can enhance bioactivity, making it a promising candidate for targeting neurological disorders and metabolic diseases. This aligns with the current trend in drug discovery, where researchers focus on small molecule therapeutics with improved selectivity and fewer side effects. The benzyl group in this compound also offers opportunities for further functionalization, expanding its utility in medicinal chemistry.

In addition to pharmaceutical applications, 3-PIPERIDINONE, 6-METHYL-1-(PHENYLMETHYL)- is explored in material science. Its rigid yet flexible structure makes it suitable for designing polymers with specific thermal and mechanical properties. This is particularly relevant given the rising interest in high-performance materials for electronics, coatings, and adhesives. Companies are investing in R&D to leverage such compounds for next-generation products.

From an analytical perspective, characterizing CAS No. 83413-42-7 involves techniques like NMR spectroscopy, mass spectrometry, and HPLC. These methods ensure purity and consistency, which are critical for regulatory compliance and industrial use. Quality control is a recurring theme in user queries, highlighting the need for reliable suppliers and standardized testing protocols.

Lastly, the market trends for 3-PIPERIDINONE derivatives indicate steady growth, driven by demand from the pharmaceutical and agrochemical sectors. As patents expire and generic alternatives emerge, cost-effective synthesis routes become increasingly valuable. This compound’s adaptability ensures its relevance in evolving scientific and industrial landscapes.

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