structure of 2-(4-methylpyridin-3-yl)ethan-1-amine

2-(4-methylpyridin-3-yl)ethan-1-amine

CAS No.: 1000504-51-7
M. Wt: 136.19400
M. Fa: C8H12N2
InChI Key: UGBWPAWWWLLZIO-UHFFFAOYSA-N

Names and Identifiers of 2-(4-methylpyridin-3-yl)ethan-1-amine

CAS Number

1000504-51-7

MDL Number

MFCD09924452

IUPAC Name

2-(4-methylpyridin-3-yl)ethan-1-amine

InChI

InChI=1S/C8H12N2/c1-7-3-5-10-6-8(7)2-4-9/h3,5-6H,2,4,9H2,1H3

InChIKey

UGBWPAWWWLLZIO-UHFFFAOYSA-N

Canonical SMILES

CC1=CC=NC=C1CCN

UNSPSC Code

12352100

Physical and chemical properties of 2-(4-methylpyridin-3-yl)ethan-1-amine

Exact Mass

136.10000

H Bond Acceptors

2

H Bond Donors

1

LogP

1.59150

Molecular Formula

C8H12N2

Molecular Weight

136.19400

PSA

38.91000

Safety Information of 2-(4-methylpyridin-3-yl)ethan-1-amine

Pictograms

Signal Word

 Danger

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

Applications of 2-(4-methylpyridin-3-yl)ethan-1-amine

2-(4-Methylpyridin-3-YL)ethanamine has diverse applications:

  • In Chemistry: It serves as a building block for synthesizing more complex organic molecules.
  • In Biology: The compound is utilized in enzyme interaction studies and as a ligand in receptor binding assays.
  • In Industry: It finds applications in the production of agrochemicals and other industrial chemicals due to its reactivity and functionalization potential.

Interaction Studies of 2-(4-methylpyridin-3-yl)ethan-1-amine

Interaction studies involving 2-(4-Methylpyridin-3-YL)ethanamine focus on its binding affinity to various biological targets. These studies are crucial for understanding its mechanism of action and optimizing its pharmacological profile. For instance, research has highlighted its potential interactions with enzymes implicated in metabolic pathways related to cancer, emphasizing its relevance in drug discovery.

Biological Activity of 2-(4-methylpyridin-3-yl)ethan-1-amine

The biological activity of 2-(4-Methylpyridin-3-YL)ethanamine is significant in medicinal chemistry. It has been studied for its potential interactions with various biological targets, including enzymes and receptors. The ethylamine moiety allows for hydrogen bonding with active sites, while the pyridine ring can engage in π-π interactions with aromatic residues. These interactions may modulate the activity of target molecules, leading to various pharmacological effects. Research indicates that derivatives of this compound may exhibit activity against certain cancer cell lines, suggesting its potential role in targeted therapies.