2-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)acetic acid
Names and Identifiers of 1000522-34-8
CAS Number |
1000522-34-8 |
|---|---|
MDL Number |
MFCD09925056 |
IUPAC Name |
2-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]acetic acid |
InChI |
InChI=1S/C8H5ClF3NO2/c9-5-1-4(8(10,11)12)3-13-6(5)2-7(14)15/h1,3H,2H2,(H,14,15) |
InChIKey |
ZCMWOZJSLGQSQV-UHFFFAOYSA-N |
Canonical SMILES |
C1=C(C=NC(=C1Cl)CC(=O)O)C(F)(F)F |
UNII |
M8LA01CDAP |
UNSPSC Code |
12352100 |
Physical and chemical properties of 1000522-34-8
Exact Mass |
238.99600 |
|---|---|
LogP |
2.38090 |
Molecular Formula |
C8H5ClF3NO2 |
Molecular Weight |
239.57900 |
PSA |
50.19000 |
Storage condition |
2-8°C |
Safety Information of 1000522-34-8
Applications of 1000522-34-8
The applications of 2-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)acetic acid are primarily found in:
- Agricultural Chemicals: Its potential as a herbicide or fungicide derivative makes it valuable in crop protection.
- Pharmaceuticals: The unique structure may lead to new drug candidates targeting various diseases.
Research into its efficacy and safety profiles continues to expand its potential applications in these fields.
Interaction Studies of 1000522-34-8
Interaction studies indicate that compounds similar to 2-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)acetic acid often engage with biological targets such as enzymes and receptors.
Mechanism of ActionWhile specific interactions for this compound are not well-documented, it is hypothesized that the trifluoromethyl group enhances binding affinity to biological targets, potentially affecting cellular signaling pathways.
Biochemical PathwaysSimilar compounds have been shown to modulate pathways involved in inflammation and cancer progression, suggesting that this compound may exhibit comparable effects.
Biological Activity of 1000522-34-8
- Antimicrobial Activity: Compounds with similar structures have shown effectiveness against microbial strains.
- Anti-inflammatory Properties: Some derivatives have been investigated for their potential to reduce inflammation.
- Anticancer Activity: Research indicates that related pyridine derivatives may influence cancer cell proliferation and survival pathways.
