structure of 3-(3-Methylpyridin-2-yl)propan-1-amine

3-(3-Methylpyridin-2-yl)propan-1-amine

CAS No.: 1000512-96-8
M. Wt: 150.22
M. Fa: C9H14N2
InChI Key: WAUXGDVCSRTHRN-UHFFFAOYSA-N

Names and Identifiers of 3-(3-Methylpyridin-2-yl)propan-1-amine

CAS Number

1000512-96-8

IUPAC Name

3-(3-methylpyridin-2-yl)propan-1-amine

InChI

InChI=1S/C9H14N2/c1-8-4-3-7-11-9(8)5-2-6-10/h3-4,7H,2,5-6,10H2,1H3

InChIKey

WAUXGDVCSRTHRN-UHFFFAOYSA-N

Canonical SMILES

CC1=C(N=CC=C1)CCCN

Physical and chemical properties of 3-(3-Methylpyridin-2-yl)propan-1-amine

Acidity coefficient

9.90±0.10(Predicted)

Boiling Point

253.4±28.0 °C(Predicted)

Density

0.988±0.06 g/cm3(Predicted)

Molecular Formula

C9H14N2

Molecular Weight

150.22

Applications of 3-(3-Methylpyridin-2-yl)propan-1-amine

The applications of 3-(3-Methylpyridin-2-yl)propan-1-amine span various fields:

  • Chemistry: It serves as a building block in organic synthesis for creating more complex molecules.
  • Biology: The compound is utilized in studies related to enzyme inhibition and receptor interactions.
  • Industry: It is employed in the production of specialty chemicals and intermediates for diverse industrial processes.

Interaction Studies of 3-(3-Methylpyridin-2-yl)propan-1-amine

Interaction studies indicate that 3-(3-Methylpyridin-2-yl)propan-1-amine may exhibit significant interactions with various biological targets. These interactions are essential for understanding its pharmacological potential and therapeutic applications. Ongoing research aims to elucidate these interactions further, which could lead to new insights into drug design and efficacy.

Biological Activity of 3-(3-Methylpyridin-2-yl)propan-1-amine

Research indicates that 3-(3-Methylpyridin-2-yl)propan-1-amine exhibits significant biological activities. It interacts with various receptors and enzymes, contributing to its pharmacological effects. Notably, studies have explored its potential role in enzyme inhibition and receptor binding, which are critical for drug development and therapeutic applications. The compound's biological profile suggests it may be beneficial in treating conditions where modulation of these targets is necessary.