structure of 2-(6-(Trifluoromethyl)pyridin-2-yl)acetic acid

2-(6-(Trifluoromethyl)pyridin-2-yl)acetic acid

CAS No.: 1000565-32-1
M. Wt: 205.13400
M. Fa: C8H6F3NO2
InChI Key: WRPOGLABYJEOEX-UHFFFAOYSA-N

Names and Identifiers of 1000565-32-1

CAS Number

1000565-32-1

MDL Number

MFCD09924928

IUPAC Name

2-[6-(trifluoromethyl)pyridin-2-yl]acetic acid

InChI

InChI=1S/C8H6F3NO2/c9-8(10,11)6-3-1-2-5(12-6)4-7(13)14/h1-3H,4H2,(H,13,14)

InChIKey

WRPOGLABYJEOEX-UHFFFAOYSA-N

Canonical SMILES

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

UNSPSC Code

12352100

Physical and chemical properties of 1000565-32-1

Exact Mass

205.03500

LogP

1.72750

Molecular Formula

C8H6F3NO2

Molecular Weight

205.13400

PSA

50.19000

Storage condition

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C

Safety Information of 1000565-32-1

Pictograms

Signal Word

 Warning

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

Applications of 1000565-32-1

The primary applications of 2-(6-(Trifluoromethyl)pyridin-2-yl)acetic acid include:

  • Pharmaceutical Development: As an intermediate in drug synthesis.
  • Agricultural Chemistry: Potential use in developing agrochemicals due to its biological activity.
  • Material Science: Used in creating novel materials with specific functional properties.

Interaction Studies of 1000565-32-1

Interaction studies have shown that 2-(6-(Trifluoromethyl)pyridin-2-yl)acetic acid can interact with various biological targets, making it a candidate for further pharmacological studies. Its interactions often depend on the presence of the trifluoromethyl group, which influences binding affinity and selectivity towards specific receptors or enzymes.

Biological Activity of 1000565-32-1

Research indicates that 2-(6-(Trifluoromethyl)pyridin-2-yl)acetic acid exhibits biological activities that may be beneficial in pharmacological applications. It has been noted for its potential as a precursor in the synthesis of microbicides and other biologically active compounds. The trifluoromethyl group is known to enhance the lipophilicity and metabolic stability of compounds, potentially increasing their efficacy as drugs.