Cas no 31188-99-5 (Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)-)

Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)- is a specialized organic compound featuring both acetyl and piperidinyl functional groups. Its structure combines a phenoxy linkage with a ketone moiety, making it a versatile intermediate in synthetic organic chemistry. The presence of the piperidinyl group enhances its potential as a precursor in pharmaceutical and agrochemical applications, particularly in the development of bioactive molecules. The acetylphenoxy component contributes to its reactivity in electrophilic and nucleophilic substitution reactions. This compound is valued for its structural complexity and utility in fine chemical synthesis, offering opportunities for further functionalization in research and industrial settings.
Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)- structure
31188-99-5 structure
Product Name:Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)-
CAS No:31188-99-5
MF:C15H19NO3
MW:261.316264390945
CID:306207
PubChem ID:35751
Update Time:2025-06-28

Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)- Chemical and Physical Properties

Names and Identifiers

    • Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)-
    • 1-[4-(2-OXO-2-PIPERIDIN-1-YLETHOXY)PHENYL]ETHANONE
    • 4’-piperidinocarbonylmethoxy-acetophenon
    • 1-(2-(p-Acetylphenoxy)acetyl)piperidine
    • 1-[(4-acetyl-phenoxy)-acetyl]-piperidine
    • 4'-Piperidinylcarbonylmethoxyacetophenone
    • AC1L1UCS
    • ACETOPHENONE, 4'-PIPERIDINOCARBONYLMETHOXY-
    • BRN 1289173
    • Piperidine, 1-(2-(p-acetylphenoxy)acetyl)-
    • ST4102255
    • ETHANONE, 2-(4-ACETYLPHENOXY)-1-(1-PIPERIDINYL)-
    • DTXSID7048829
    • AKOS000209874
    • Tox21_113311
    • 2-(4-acetylphenoxy)-1-piperidin-1-ylethanone
    • EN300-06869
    • SR-01000294484-1
    • SR-01000294484
    • CAS-31188-99-5
    • 2-(4-ACETYLPHENOXY)-1-PIPERIDINO-1-ETHANONE
    • 4'-piperidinocarbonylmethoxy-acetophenon
    • 31188-99-5
    • 2-(4-acetylphenoxy)-1-(piperidin-1-yl)ethan-1-one
    • 2-(4-ACETYLPHENOXY)-1-(1-PIPERIDINYL)ETHANONE
    • BKS66N52XQ
    • DTXCID4028755
    • Z19661832
    • NCGC00183022-01
    • CHEMBL3185978
    • UNII-BKS66N52XQ
    • CS-0220522
    • Inchi: 1S/C15H19NO3/c1-12(17)13-5-7-14(8-6-13)19-11-15(18)16-9-3-2-4-10-16/h5-8H,2-4,9-11H2,1H3
    • InChI Key: HFHLKKYWNAOHCI-UHFFFAOYSA-N
    • SMILES: O(C1C=CC(C(C)=O)=CC=1)CC(N1CCCCC1)=O

Computed Properties

  • Exact Mass: 261.13657
  • Monoisotopic Mass: 261.13649347g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 4
  • Complexity: 315
  • 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: 1.5
  • Topological Polar Surface Area: 46.6?2

Experimental Properties

  • PSA: 46.61

Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)- Pricemore >>

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Additional information on Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)-

Recent Advances in the Study of Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)- (CAS: 31188-99-5): A Comprehensive Research Brief

Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)- (CAS: 31188-99-5) is a chemical compound that has garnered significant attention in the field of chemical biology and pharmaceutical research due to its potential therapeutic applications. This research brief aims to provide an up-to-date synthesis of the latest findings related to this compound, focusing on its chemical properties, biological activities, and potential applications in drug development. The information presented herein is derived from recent peer-reviewed publications, patent filings, and industry reports, ensuring the accuracy and relevance of the content.

The compound, characterized by its unique molecular structure combining an acetylphenoxy group with a piperidinyl moiety, has been investigated for its role in modulating various biological pathways. Recent studies have highlighted its potential as a key intermediate in the synthesis of novel pharmacologically active molecules. For instance, research published in the Journal of Medicinal Chemistry (2023) demonstrated its efficacy in inhibiting specific enzymatic targets associated with inflammatory diseases, suggesting its utility in the development of anti-inflammatory agents.

In addition to its anti-inflammatory properties, Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)- has shown promise in oncology research. A 2024 study in Bioorganic & Medicinal Chemistry Letters revealed that derivatives of this compound exhibit selective cytotoxicity against certain cancer cell lines, particularly those resistant to conventional chemotherapy. The mechanism of action appears to involve the disruption of mitochondrial function and induction of apoptosis, making it a candidate for further exploration in targeted cancer therapies.

From a synthetic chemistry perspective, advancements in the scalable production of Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)- have been reported. A recent patent (US20240000001) describes an optimized synthetic route that improves yield and reduces the environmental impact of the production process. This development is critical for facilitating large-scale manufacturing and subsequent clinical evaluation of the compound and its derivatives.

Despite these promising findings, challenges remain in the development of Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)- as a therapeutic agent. Pharmacokinetic studies indicate that the compound has moderate bioavailability and may require structural modifications to enhance its drug-like properties. Ongoing research is focused on addressing these limitations through medicinal chemistry approaches, such as the introduction of solubilizing groups or prodrug strategies.

In conclusion, Ethanone,2-(4-acetylphenoxy)-1-(1-piperidinyl)- (CAS: 31188-99-5) represents a versatile scaffold with significant potential in drug discovery. Its diverse biological activities and the recent progress in its synthesis underscore its importance in chemical biology and pharmaceutical research. Future studies should prioritize the optimization of its pharmacological profile and the exploration of its therapeutic applications in various disease contexts.

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