Cas no 1003560-59-5 (2-(Piperidin-3-yl)propan-2-ol hydrochloride)

2-(Piperidin-3-yl)propan-2-ol hydrochloride is a versatile organic compound featuring a piperidine core with a tertiary alcohol substituent, rendered as its hydrochloride salt for enhanced stability and solubility. This structural motif is valuable in medicinal chemistry, particularly as a building block for the synthesis of pharmacologically active molecules. The hydrochloride form ensures improved handling and storage characteristics. The compound’s piperidine scaffold is frequently employed in the development of CNS-targeting agents, while the hydroxyl group offers a reactive site for further derivatization. Its well-defined purity and consistent quality make it suitable for research applications in drug discovery and development.
2-(Piperidin-3-yl)propan-2-ol hydrochloride structure
1003560-59-5 structure
Product Name:2-(Piperidin-3-yl)propan-2-ol hydrochloride
CAS No:1003560-59-5
MF:C8H18ClNO
MW:179.687621593475
CID:4558685
Update Time:2025-05-21

2-(Piperidin-3-yl)propan-2-ol hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2-(piperidin-3-yl)propan-2-ol hydrochloride
    • 2-piperidin-3-ylpropan-2-ol hydrochloride
    • 2-piperidin-3-ylpropan-2-ol;hydrochloride
    • 3-(1-methyl-1-hydroxyethyl)piperidine hydrochloride
    • Z2756332631
    • 2-(Piperidin-3-yl)propan-2-ol hydrochloride
    • Inchi: 1S/C8H17NO.ClH/c1-8(2,10)7-4-3-5-9-6-7;/h7,9-10H,3-6H2,1-2H3;1H
    • InChI Key: SEDMILKWVAVRIH-UHFFFAOYSA-N
    • SMILES: Cl.OC(C)(C)C1CNCCC1

Computed Properties

  • Exact Mass: 179.107692g/mol
  • Monoisotopic Mass: 179.107692g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 112
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Molecular Weight: 179.69g/mol
  • Topological Polar Surface Area: 32.299

2-(Piperidin-3-yl)propan-2-ol hydrochloride Pricemore >>

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Additional information on 2-(Piperidin-3-yl)propan-2-ol hydrochloride

2-(Piperidin-3-yl)propan-2-ol hydrochloride

2-(Piperidin-3-yl)propan-2-ol hydrochloride, also known by its CAS number 1003560-59-5, is a compound of significant interest in the fields of organic chemistry and pharmaceutical research. This compound is a hydrochloride salt of 2-(piperidin-3-yl)propan-2-ol, which is a tertiary alcohol derivative of piperidine, a six-membered saturated heterocyclic amine. The structure of this compound is characterized by a piperidine ring substituted at the third position with a propanol group, resulting in a unique stereochemistry and reactivity.

The synthesis of 1003560-59-5 typically involves multi-step organic reactions, including nucleophilic substitution, reduction, and acid-base neutralization. The compound has been studied for its potential applications in drug design, particularly as a precursor or intermediate in the synthesis of bioactive molecules. Recent research has highlighted its role in the development of novel therapeutic agents targeting various biological pathways, including those involved in inflammation, pain management, and neurodegenerative diseases.

One of the key features of 2-(Piperidin-3-yl)propan-2-ol hydrochloride is its ability to act as a chiral auxiliary or catalyst in asymmetric synthesis. This property has made it valuable in the construction of complex molecular architectures with high enantioselectivity. Additionally, the compound exhibits interesting pharmacokinetic properties, making it a promising candidate for drug delivery systems.

Recent studies have also explored the interaction of 1003560-59-5 with biological macromolecules such as proteins and nucleic acids. These investigations have provided insights into its potential as a modulator of enzyme activity or as a component in gene therapy vectors. Furthermore, the compound has been evaluated for its antioxidant and anti-inflammatory properties, which could be harnessed in the development of nutraceuticals and cosmeceuticals.

In terms of industrial applications, 2-(Piperidin-3-yl)propan-2-ol hydrochloride has found utility in the formulation of specialty chemicals and advanced materials. Its ability to participate in various chemical transformations under mild conditions makes it an attractive building block for material scientists and process engineers.

The growing interest in 1003560-59-5 can be attributed to its versatile chemical properties and the increasing demand for innovative solutions in healthcare and materials science. As research continues to uncover new aspects of this compound's behavior and functionality, it is expected to play an even more prominent role in both academic and industrial settings.

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