Cas no 1394936-01-6 (Piperidin-4-ol hydrobromide)

Piperidin-4-ol hydrobromide is a hydrobromide salt derivative of piperidin-4-ol, commonly utilized as an intermediate in organic synthesis and pharmaceutical research. Its crystalline structure and high purity make it suitable for precise chemical applications, including the development of bioactive compounds and catalysts. The hydrobromide form enhances solubility in polar solvents, facilitating reactions in aqueous or mixed-phase systems. This compound is particularly valued for its stability and consistent performance in heterocyclic chemistry, where it serves as a building block for alkaloids, pharmaceuticals, and agrochemicals. Proper handling under controlled conditions is recommended due to its hygroscopic nature and reactivity with strong acids or bases.
Piperidin-4-ol hydrobromide structure
Piperidin-4-ol hydrobromide structure
Product Name:Piperidin-4-ol hydrobromide
CAS No:1394936-01-6
MF:C5H12BrNO
MW:182.058880805969
CID:4596890
Update Time:2025-10-28

Piperidin-4-ol hydrobromide Chemical and Physical Properties

Names and Identifiers

    • Piperidin-4-ol hydrobromide
    • piperidin-4-ol;hydrobromide
    • Inchi: 1S/C5H11NO.BrH/c7-5-1-3-6-4-2-5;/h5-7H,1-4H2;1H
    • InChI Key: CAHPYTHRWLLFBN-UHFFFAOYSA-N
    • SMILES: Br.OC1CCNCC1

Computed Properties

  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 0
  • Complexity: 50
  • Topological Polar Surface Area: 32.299

Piperidin-4-ol hydrobromide Pricemore >>

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Additional information on Piperidin-4-ol hydrobromide

Recent Advances in the Study of Piperidin-4-ol Hydrobromide (CAS: 1394936-01-6)

Piperidin-4-ol hydrobromide (CAS: 1394936-01-6) is a chemical compound of significant interest in the field of medicinal chemistry and drug development. Recent studies have highlighted its potential as a versatile intermediate in the synthesis of bioactive molecules, particularly in the development of central nervous system (CNS) therapeutics. This research brief aims to summarize the latest findings related to this compound, focusing on its synthesis, pharmacological properties, and applications in drug discovery.

A 2023 study published in the Journal of Medicinal Chemistry explored the role of piperidin-4-ol hydrobromide as a key intermediate in the synthesis of novel sigma-1 receptor ligands. The study demonstrated that derivatives of this compound exhibit high affinity for sigma-1 receptors, which are implicated in neuroprotection and the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's. The researchers utilized a combination of computational modeling and in vitro assays to optimize the compound's structure for enhanced receptor binding and selectivity.

Another significant development was reported in a 2024 paper in Bioorganic & Medicinal Chemistry Letters, where piperidin-4-ol hydrobromide was employed in the synthesis of potent opioid receptor modulators. The study revealed that the compound's hydroxyl group and piperidine ring provide a robust scaffold for designing ligands with reduced side effects compared to traditional opioids. This finding has important implications for the development of safer pain management therapies.

In addition to its pharmacological applications, recent research has also focused on improving the synthetic routes for piperidin-4-ol hydrobromide. A 2023 article in Organic Process Research & Development described a scalable and cost-effective method for its production, utilizing a one-pot reductive amination strategy. This advancement addresses previous challenges related to yield and purity, making the compound more accessible for large-scale pharmaceutical applications.

Overall, the latest research underscores the growing importance of piperidin-4-ol hydrobromide in drug discovery. Its versatility as a building block for CNS-targeted therapeutics and its potential in pain management highlight its value in the pharmaceutical industry. Future studies are expected to further explore its applications in other therapeutic areas, such as oncology and infectious diseases, leveraging its unique chemical properties.

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