Cas no 155826-26-9 (1-Acetylpiperidine-4-carbaldehyde)

1-Acetylpiperidine-4-carbaldehyde structure
155826-26-9 structure
Product Name:1-Acetylpiperidine-4-carbaldehyde
CAS No:155826-26-9
MF:C8H13NO2
MW:155.194322347641
MDL:MFCD11582881
CID:107160
PubChem ID:18428037
Update Time:2025-10-29

1-Acetylpiperidine-4-carbaldehyde Chemical and Physical Properties

Names and Identifiers

    • 1-Acetylpiperidine-4-carbaldehyde
    • 1-Acetyl-4-piperidinecarboxaldehyde
    • 4-FORMYLPIPERIDINE
    • 4-PIPERIDINECARBOXALDEHYDE, 1-ACETYL- (9CI)
    • 4-Piperidinecarboxaldehyde,1-acetyl-
    • Piperidine-4-carbaldehyde
    • 1-Acetyl-piperidine-4-carbaldehyde
    • AK-67866
    • AM100297
    • ANW-71819
    • CTK8C4415
    • N-acetylpiperidine-4-carbaldehyde
    • N-acetylpiperidine-4-carboxaldehyde
    • 4-Piperidinecarboxal
    • UQEFRJJPHHMUQP-UHFFFAOYSA-N
    • DTXSID00593684
    • SY101845
    • SCHEMBL57712
    • MFCD11582881
    • AKOS006283924
    • SB41345
    • AS-44870
    • EN300-240356
    • A883616
    • AB8006
    • Z1116428589
    • F2147-1743
    • 4-Piperidinecarboxaldehyde, 1-acetyl-
    • CS-W006375
    • FT-0769304
    • 155826-26-9
    • DA-09859
    • MDL: MFCD11582881
    • Inchi: 1S/C8H13NO2/c1-7(11)9-4-2-8(6-10)3-5-9/h6,8H,2-5H2,1H3
    • InChI Key: UQEFRJJPHHMUQP-UHFFFAOYSA-N
    • SMILES: O=CC1CCN(C(C)=O)CC1

Computed Properties

  • Exact Mass: 155.09469
  • Monoisotopic Mass: 155.094628657g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 160
  • 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: -0.3
  • Topological Polar Surface Area: 37.4?2

Experimental Properties

  • PSA: 37.38

1-Acetylpiperidine-4-carbaldehyde Pricemore >>

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Additional information on 1-Acetylpiperidine-4-carbaldehyde

1-Acetylpiperidine-4-carbaldehyde (CAS No. 155826-26-9): A Versatile Building Block in Organic Synthesis

1-Acetylpiperidine-4-carbaldehyde (CAS No. 155826-26-9) is a highly valuable heterocyclic compound that has gained significant attention in pharmaceutical and fine chemical industries. This piperidine derivative serves as a crucial intermediate for the synthesis of various bioactive molecules, particularly in the development of central nervous system (CNS) drugs and enzyme inhibitors.

The molecular structure of 1-Acetylpiperidine-4-carbaldehyde features both acetyl and aldehyde functional groups attached to a piperidine ring, making it a versatile building block for organic synthesis. Recent studies highlight its importance in creating novel drug candidates, especially those targeting neurological disorders - a hot topic in current medicinal chemistry research.

In the pharmaceutical sector, 1-Acetylpiperidine-4-carbaldehyde 155826-26-9 is frequently used as a precursor for N-heterocyclic compounds with potential therapeutic applications. Researchers are particularly interested in its role in developing cognitive enhancers and neuroprotective agents, addressing the growing demand for treatments related to age-related cognitive decline - a major concern in aging populations worldwide.

The synthetic applications of this compound extend beyond pharmaceuticals. It serves as a key intermediate in the production of specialty chemicals used in flavor and fragrance industries. The aldehyde functionality allows for various condensation reactions, making it valuable for creating complex molecular architectures - a technique gaining popularity in green chemistry approaches.

From a market perspective, the demand for 1-Acetylpiperidine-4-carbaldehyde has been steadily increasing, particularly from contract research organizations and drug discovery companies. The compound's versatility aligns well with current trends in fragment-based drug design and combinatorial chemistry, answering frequent search queries about "building blocks for drug discovery."

Quality control of 1-Acetylpiperidine-4-carbaldehyde 155826-26-9 is crucial for research applications. Reputable suppliers typically provide high-purity grades (>98%) with comprehensive analytical data, including HPLC and NMR spectra. This ensures reproducibility in experimental results - a critical factor for researchers frequently searching for "reliable chemical intermediates."

The storage and handling of this compound require standard laboratory precautions. While not classified as hazardous under normal conditions, it should be stored in cool, dry conditions to maintain stability. This practical information addresses common user queries about "chemical storage best practices" in research settings.

Recent scientific publications have highlighted novel synthetic routes to 1-Acetylpiperidine-4-carbaldehyde, focusing on catalytic methods and atom-efficient processes. These advancements respond to the growing interest in sustainable chemistry solutions, a trending topic in both academic and industrial chemistry circles.

For researchers exploring structure-activity relationships, the piperidine-4-carbaldehyde scaffold offers excellent opportunities for molecular modification. This aspect makes the compound particularly valuable in lead optimization studies, addressing frequent search terms like "scaffolds for drug design."

In conclusion, 1-Acetylpiperidine-4-carbaldehyde (CAS 155826-26-9) represents an important chemical intermediate with wide-ranging applications in drug discovery and specialty chemical synthesis. Its unique structural features and versatility continue to make it a valuable tool for researchers developing next-generation therapeutics and functional materials.

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