structure of 2-(6-Trifluoromethyl-pyridin-2-YL)-ethylamine

2-(6-Trifluoromethyl-pyridin-2-YL)-ethylamine

CAS No.: 1000504-55-1
M. Wt: 190.16600
M. Fa: C8H9F3N2
InChI Key: CUMPHXGSZPTDQH-UHFFFAOYSA-N

Names and Identifiers of 1000504-55-1

CAS Number

1000504-55-1

MDL Number

MFCD09924461

IUPAC Name

2-[6-(trifluoromethyl)pyridin-2-yl]ethanamine

InChI

InChI=1S/C8H9F3N2/c9-8(10,11)7-3-1-2-6(13-7)4-5-12/h1-3H,4-5,12H2

InChIKey

CUMPHXGSZPTDQH-UHFFFAOYSA-N

Canonical SMILES

C1=CC(=NC(=C1)C(F)(F)F)CCN

UNSPSC Code

12352100

Physical and chemical properties of 1000504-55-1

Exact Mass

190.07200

H Bond Acceptors

2

H Bond Donors

1

LogP

2.30190

Molecular Formula

C8H9F3N2

Molecular Weight

190.16600

PSA

38.91000

Safety Information of 1000504-55-1

Pictograms

Signal Word

 Warning

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

Applications of 1000504-55-1

The applications of 2-(6-Trifluoromethyl-pyridin-2-YL)-ethylamine extend across various fields:

  • Pharmaceuticals: It serves as an intermediate in the synthesis of pharmaceutical agents, particularly those targeting neurological disorders or infections.
  • Agrochemicals: The compound is also explored for use in crop protection products due to its potential efficacy against pests and diseases.
  • Material Science: Its unique chemical properties make it suitable for developing advanced materials with specific functionalities.

Interaction Studies of 1000504-55-1

Interaction studies involving 2-(6-Trifluoromethyl-pyridin-2-YL)-ethylamine are crucial for understanding its biological mechanisms. These studies often focus on:

  • Binding Affinity: Evaluating how well the compound binds to biological targets such as enzymes or receptors.
  • Synergistic Effects: Investigating how this compound interacts with other drugs or compounds to enhance therapeutic effects.
  • Toxicity Profiles: Assessing potential toxicity and side effects associated with its biological activity.

Biological Activity of 1000504-55-1

The biological activity of 2-(6-Trifluoromethyl-pyridin-2-YL)-ethylamine is still under investigation, but preliminary studies suggest that it may exhibit pharmacological properties similar to other pyridine derivatives. Compounds with trifluoromethyl groups are often associated with increased lipophilicity and bioactivity, making them valuable in drug design. Research indicates potential applications in:

  • Antimicrobial Agents: Similar compounds have shown efficacy against various bacterial strains.
  • Anticancer Activity: Some derivatives have been explored for their ability to inhibit cancer cell proliferation.