structure of 2-(5-Fluoropyridin-3-YL)ethanamine

2-(5-Fluoropyridin-3-YL)ethanamine

CAS No.: 1000537-08-5
M. Wt: 140.15800
M. Fa: C7H9FN2
InChI Key: KYEMPLCYHAFSAY-UHFFFAOYSA-N

Names and Identifiers of 2-(5-Fluoropyridin-3-YL)ethanamine

CAS Number

1000537-08-5

MDL Number

MFCD09924497

IUPAC Name

2-(5-fluoropyridin-3-yl)ethanamine

InChI

InChI=1S/C7H9FN2/c8-7-3-6(1-2-9)4-10-5-7/h3-5H,1-2,9H2

InChIKey

KYEMPLCYHAFSAY-UHFFFAOYSA-N

Canonical SMILES

C1=C(C=NC=C1F)CCN

UNSPSC Code

12352100

Physical and chemical properties of 2-(5-Fluoropyridin-3-YL)ethanamine

Exact Mass

140.07500

H Bond Acceptors

2

H Bond Donors

1

LogP

1.42220

Molecular Formula

C7H9FN2

Molecular Weight

140.15800

PSA

38.91000

Safety Information of 2-(5-Fluoropyridin-3-YL)ethanamine

Pictograms

Signal Word

 Warning

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

Applications of 2-(5-Fluoropyridin-3-YL)ethanamine

2-(5-Fluoropyridin-3-YL)ethanamine has diverse applications across various fields:

  • Medicinal Chemistry: It serves as a building block in the synthesis of pharmaceuticals targeting specific receptors or enzymes.
  • Agricultural Chemistry: The compound is explored for use in developing agrochemicals.
  • Material Science: Its unique properties make it valuable in synthesizing new materials with specific functionalities.

Interaction Studies of 2-(5-Fluoropyridin-3-YL)ethanamine

Studies on 2-(5-Fluoropyridin-3-YL)ethanamine reveal its affinity towards specific molecular targets such as enzymes and receptors. The presence of the fluorine atom enhances binding selectivity and potency, which is critical for drug design. Ongoing research aims to elucidate the precise mechanisms by which this compound exerts its biological effects.

Biological Activity of 2-(5-Fluoropyridin-3-YL)ethanamine

Research indicates that 2-(5-Fluoropyridin-3-YL)ethanamine exhibits potential biological activities, particularly in antimicrobial and anticancer domains. The fluorine atom enhances its binding affinity to biological targets, making it a candidate for drug development. Its mechanism of action is believed to involve interactions with specific enzymes or receptors, where the unique electronic properties imparted by the fluorine atom play a crucial role.