Cas no 88796-04-7 (Ethanone, 1-[1-(phenylmethyl)-4-piperidinyl]-)

Ethanone, 1-[1-(phenylmethyl)-4-piperidinyl]-, is a synthetic organic compound featuring a piperidine core substituted with a benzyl group at the nitrogen and an acetyl group at the 4-position. This structure imparts versatility in pharmaceutical and chemical synthesis applications, particularly as an intermediate in the development of bioactive molecules. The compound's well-defined reactivity profile, attributed to the ketone and tertiary amine functionalities, enables selective modifications for tailored derivatives. Its stability under standard conditions and compatibility with common organic solvents enhance its utility in multistep syntheses. The benzyl-piperidine scaffold is of interest in medicinal chemistry due to its potential interactions with biological targets, making this compound valuable for research and drug discovery.
Ethanone, 1-[1-(phenylmethyl)-4-piperidinyl]- structure
88796-04-7 structure
Product Name:Ethanone, 1-[1-(phenylmethyl)-4-piperidinyl]-
CAS No:88796-04-7
MF:C14H19NO
MW:217.306763887405
CID:1931030
PubChem ID:910923
Update Time:2025-06-15

Ethanone, 1-[1-(phenylmethyl)-4-piperidinyl]- Chemical and Physical Properties

Names and Identifiers

    • Ethanone, 1-[1-(phenylmethyl)-4-piperidinyl]-
    • 1-(1-benzylpiperidin-4-yl)ethanone
    • ZTTPDEBBWJUCQQ-UHFFFAOYSA-N
    • 1-(1-Benzyl-piperidin-4-yl)-ethanone
    • 1-benzyl-4-acetylpiperidine
    • 88796-04-7
    • DB-316170
    • MLS000552493
    • AKOS013157786
    • 1-(1-Benzylpiperidin-4-yl)ethan-1-one
    • DTXSID10358706
    • SMR000146008
    • SCHEMBL592839
    • 4-acetyl-1-benzylpiperidine
    • HMS2305B05
    • CHEMBL1430254
    • STL322006
    • CS-0322055
    • Inchi: 1S/C14H19NO/c1-12(16)14-7-9-15(10-8-14)11-13-5-3-2-4-6-13/h2-6,14H,7-11H2,1H3
    • InChI Key: ZTTPDEBBWJUCQQ-UHFFFAOYSA-N
    • SMILES: O=C(C)C1CCN(CC2C=CC=CC=2)CC1

Computed Properties

  • Exact Mass: 217.146664230Da
  • Monoisotopic Mass: 217.146664230Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 3
  • Complexity: 225
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.9
  • Topological Polar Surface Area: 20.3?2

Ethanone, 1-[1-(phenylmethyl)-4-piperidinyl]- Pricemore >>

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Additional information on Ethanone, 1-[1-(phenylmethyl)-4-piperidinyl]-

Comprehensive Overview of Ethanone, 1-[1-(phenylmethyl)-4-piperidinyl]- (CAS No. 88796-04-7)

Ethanone, 1-[1-(phenylmethyl)-4-piperidinyl]-, with the CAS number 88796-04-7, is a specialized organic compound that has garnered significant attention in pharmaceutical and chemical research. This compound, also referred to by its systematic name, belongs to the class of piperidine derivatives, which are widely studied for their potential applications in drug development and material science. The presence of both phenylmethyl and piperidinyl groups in its structure makes it a versatile intermediate for synthesizing more complex molecules.

In recent years, the demand for piperidine-based compounds has surged due to their role in designing central nervous system (CNS) therapeutics. Researchers are particularly interested in how Ethanone, 1-[1-(phenylmethyl)-4-piperidinyl]- can be utilized to develop novel neuroprotective agents or cognitive enhancers. This aligns with the growing public interest in brain health and mental wellness, topics frequently searched in health forums and academic databases. The compound's unique structure allows it to interact with specific neurotransmitter receptors, making it a candidate for further exploration in neurological disorders.

From a synthetic chemistry perspective, CAS No. 88796-04-7 serves as a valuable building block. Its ketone functional group and aromatic ring provide multiple sites for chemical modifications, enabling the creation of diverse derivatives. This adaptability is crucial for medicinal chemists aiming to optimize bioavailability and target specificity in drug candidates. Searches for "piperidine derivatives in drug discovery" or "ketone-based pharmaceuticals" often highlight the importance of compounds like this one.

Another area where Ethanone, 1-[1-(phenylmethyl)-4-piperidinyl]- finds relevance is in flavor and fragrance industries. The compound's molecular framework can contribute to the synthesis of aromatic compounds used in perfumes and food additives. This application ties into the broader trend of natural and synthetic aroma chemicals, a topic frequently discussed in consumer product forums and industrial chemistry publications.

Environmental and safety considerations are also critical when discussing CAS No. 88796-04-7. While not classified as a hazardous substance, proper handling protocols are essential to ensure workplace safety. This aligns with the increasing public interest in green chemistry and sustainable manufacturing, as seen in searches for "eco-friendly chemical synthesis" and "safe laboratory practices".

In summary, Ethanone, 1-[1-(phenylmethyl)-4-piperidinyl]- (88796-04-7) is a multifaceted compound with applications spanning pharmaceuticals, flavor chemistry, and material science. Its structural features and reactivity make it a subject of ongoing research, particularly in fields addressing neurological health and sustainable chemistry. As interest in these areas grows, so does the relevance of this compound in both academic and industrial settings.

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