structure of 3-(9H-carbazol-9-yl)propan-1-amine hydrochloride

3-(9H-carbazol-9-yl)propan-1-amine hydrochloride

CAS No.: 1001349-06-9
M. Wt: 260.76188
M. Fa: C15H17ClN2
InChI Key: -

Names and Identifiers of 1001349-06-9

CAS Number

1001349-06-9

IUPAC Name

3-carbazol-9-ylpropan-1-amine;hydrochloride

Canonical SMILES

C1=CC=C2C(=C1)C3=CC=CC=C3N2CCCN.Cl

Physical and chemical properties of 1001349-06-9

Melting Point

273 °C

Molecular Formula

C15H17ClN2

Molecular Weight

260.76188

Applications of 1001349-06-9

3-(9H-carbazol-9-yl)propan-1-amine hydrochloride finds applications in various fields:

  • Pharmaceutical Development: It serves as a building block for synthesizing new drugs, particularly in oncology and infectious diseases.
  • Material Science: Its unique properties allow for exploration in organic electronics and photonic devices due to the conjugated system present in carbazole derivatives.
  • Research Tool: Utilized in biochemical assays to study enzyme interactions and cellular processes related to neurodegenerative diseases.

Interaction Studies of 1001349-06-9

Interaction studies involving 3-(9H-carbazol-9-yl)propan-1-amine hydrochloride focus on its binding affinities with various biological targets:

  • Receptor Binding: Investigations into how this compound interacts with neurotransmitter receptors have shown promise in neuropharmacology.
  • Enzyme Inhibition: Studies reveal that it may inhibit certain enzymes linked to cancer progression, suggesting a potential therapeutic role.

Biological Activity of 1001349-06-9

3-(9H-carbazol-9-yl)propan-1-amine hydrochloride exhibits significant biological activity, particularly in the field of pharmacology. Research indicates that compounds containing carbazole structures often display:

  • Anticancer Properties: Some derivatives have shown potential in inhibiting cancer cell proliferation.
  • Antimicrobial Activity: The compound may possess antibacterial and antifungal properties, making it a candidate for further development in antimicrobial therapies.
  • Neuroprotective Effects: There is emerging evidence suggesting that similar compounds can protect neuronal cells from oxidative stress.