structure of 1-(2-Pyridyl)-1-propylamine

1-(2-Pyridyl)-1-propylamine

CAS No.: 100155-73-5
M. Wt: 136.19400
M. Fa: C8H12N2
InChI Key: ARIBPNACTHQUIK-UHFFFAOYSA-N
Appearance: Yellow Liquid

Names and Identifiers of 1-(2-Pyridyl)-1-propylamine

CAS Number

100155-73-5

MDL Number

MFCD09802324

IUPAC Name

1-pyridin-2-ylpropan-1-amine

InChI

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

InChIKey

ARIBPNACTHQUIK-UHFFFAOYSA-N

Canonical SMILES

CCC(C1=CC=CC=N1)N

UNSPSC Code

12352100

Physical and chemical properties of 1-(2-Pyridyl)-1-propylamine

Acidity coefficient

9.02±0.39(Predicted)

Boiling Point

214.13ºC at 760 mmHg

Density

0.998g/cm3

Exact Mass

136.10000

Flash Point

103.931ºC

Index of Refraction

1.529

LogP

2.19170

Melting Point

57 °C

Molecular Formula

C8H12N2

Molecular Weight

136.19400

PSA

38.91000

Storage condition

under inert gas (nitrogen or Argon) at 2–8 °C

Vapour Pressure

0.158mmHg at 25°C

Safety Information of 1-(2-Pyridyl)-1-propylamine

Pictograms

Signal Word

 Warning

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

Applications of 1-(2-Pyridyl)-1-propylamine

1-(2-Pyridyl)-1-propylamine finds applications in various domains:

  • Pharmaceuticals: It serves as an intermediate in the synthesis of pharmaceuticals, particularly those targeting neurological or allergic conditions.
  • Catalysis: Its derivatives are used as ligands in catalytic processes, enhancing reaction selectivity and efficiency.
  • Research: The compound is utilized in academic research to explore new synthetic methodologies and biological interactions.

Biological Activity of 1-(2-Pyridyl)-1-propylamine

The biological activity of 1-(2-Pyridyl)-1-propylamine has been explored in various studies. It has shown potential as:

  • Antihistaminic Agent: Similar compounds have been investigated for their antihistaminic properties, making this compound a candidate for further research in allergy treatments.
  • Ligand in Catalysis: Its derivatives are being studied as ligands in asymmetric catalysis, which can control the stereochemical outcomes of reactions.

Physical sample testing spectrum (NMR) of 1-(2-Pyridyl)-1-propylamine

Physical sample testing spectrum (NMR) of 1-(2-Pyridyl)-1-propylamine

Retrosynthesis analysis of 1-(2-Pyridyl)-1-propylamine

  • Route#1

    Cas:108018-18-4
    Cas:100155-73-5