structure of Piperidin-3-ylmethanol hydrochloride

Piperidin-3-ylmethanol hydrochloride

CAS No.: 400771-49-5
M. Wt: 151.63400
M. Fa: C6H14ClNO
InChI Key: VLFTUQPTEOPYGV-UHFFFAOYSA-N
Appearance: Pale-green Solid

Names and Identifiers of Piperidin-3-ylmethanol hydrochloride

CAS Number

400771-49-5

MDL Number

MFCD08752661

IUPAC Name

piperidin-3-ylmethanol;hydrochloride

InChI

InChI=1S/C6H13NO.ClH/c8-5-6-2-1-3-7-4-6;/h6-8H,1-5H2;1H

InChIKey

VLFTUQPTEOPYGV-UHFFFAOYSA-N

Canonical SMILES

C1CC(CNC1)CO.Cl

UNSPSC Code

12352100

Physical and chemical properties of Piperidin-3-ylmethanol hydrochloride

Exact Mass

151.07600

LogP

1.10910

Molecular Formula

C6H14ClNO

Molecular Weight

151.63400

PSA

32.26000

Safety Information of Piperidin-3-ylmethanol hydrochloride

Pictograms

Signal Word

Warning

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Applications of Piperidin-3-ylmethanol hydrochloride

Piperidin-3-ylmethanol hydrochloride has several applications across various fields:

  • Pharmaceuticals: It serves as an intermediate in the synthesis of drugs targeting neurological and oncological conditions.
  • Chemical Research: The compound is utilized in studies exploring structure-activity relationships in drug development.
  • Material Science: Its derivatives may find use in creating new materials with specific properties due to their unique structural attributes.

Interaction Studies of Piperidin-3-ylmethanol hydrochloride

Interaction studies involving piperidin-3-ylmethanol hydrochloride focus on its binding affinities and mechanisms of action with various biological targets:

  • Receptor Binding Studies: Investigations into how this compound interacts with neurotransmitter receptors (e.g., muscarinic acetylcholine receptors) are crucial for understanding its potential therapeutic effects.
  • Enzyme Inhibition Studies: Some derivatives have been evaluated for their ability to inhibit enzymes involved in disease processes, providing insights into their mechanisms of action and potential therapeutic roles.

Biological Activity of Piperidin-3-ylmethanol hydrochloride

Research indicates that piperidine derivatives, including piperidin-3-ylmethanol hydrochloride, exhibit various biological activities:

  • Anticancer Properties: Certain derivatives have shown cytotoxic effects against cancer cell lines, suggesting potential for development as anticancer agents.
  • Neuropharmacological Effects: Compounds containing piperidine moieties have been studied for their interactions with neurotransmitter receptors, indicating possible applications in treating neurological disorders.
  • Antimicrobial Activity: Some studies suggest that piperidine derivatives possess antimicrobial properties, making them candidates for further investigation in infectious disease treatments.

Physical sample testing spectrum (NMR) of Piperidin-3-ylmethanol hydrochloride

Physical sample testing spectrum (NMR) of Piperidin-3-ylmethanol hydrochloride