197775-45-4

Usage

Uses

Used in Pharmaceutical Industry:
5-Pyridin-4-yl-4H-pyrazole-3-carboxylic Acid is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure, containing Pyridin, Pyrazole, and Carboxylic Acid functional groups, makes it a promising candidate for the development of new drugs and therapeutic agents.
Used in Research and Development:
5-Pyridin-4-yl-4H-pyrazole-3-carboxylic Acid is used as a research compound in the field of organic chemistry. Its heterocyclic nature and functional groups provide opportunities for studying its chemical properties, reactivity, and potential applications in various chemical reactions and processes.
Used in Material Science:
5-Pyridin-4-yl-4H-pyrazole-3-carboxylic Acid may be used as a component in the development of new materials with specific properties, such as conductivity, stability, or reactivity. Its heterocyclic structure and functional groups could contribute to the creation of novel materials with potential applications in various industries.
Note: The specific applications and uses mentioned above are hypothetical and based on the general properties of heterocyclic compounds. Further research and experimentation are necessary to confirm the actual applications and benefits of 5-Pyridin-4-yl-4H-pyrazole-3-carboxylic Acid.

InChI:InChI=1/C9H7N3O2/c13-9(14)8-5-7(11-12-8)6-1-3-10-4-2-6/h1-5H,(H,11,12)(H,13,14)

Upstream product

• 1122-54-9 methyl (4-pyridyl) ketone 
• 60943-41-1 ethyl 2,4-dioxo-4-(pyridin-4-yl)butanoate 
• 19959-81-0 3-(4-pyridinyl)-1H-pyrazole-5-carboxylic acid ethyl ester 

Downstream Products

• 1354404-40-2 N-methyl-5-(pyridin-4-yl)-N-(4-(quinolin-2-ylmethyloxy)phenyl)-1H-pyrazole-3-carboxamide 

Relevant academic research and scientific papers

A novel pyridine-pyrazole based selective “turn-off” fluorescent chemosensor for Fe(III) ions

A novel pyridine-pyrazole based “turn-off” fluorescent chemosensor namely, 5-N-(pyridine-2-yl)-3-(pyridine-4-yl)-1H-pyrazole-5-carboxamide (PPPC) was designed, synthesized and well characterized by NMR, ESI-MS and FT-IR spectroscopic techniques. UV–vis absorption and fluorescence spectroscopic studies show that PPPC exhibits high selectivity and sensitivity towards Fe3+ ion in DMSO/H2O solution (9:1, v/v) over other metal ions. The binding constant (K) of PPPC with Fe3+ was calculated to be 5.1 × 10?2 M and 6.1 × 10?2 M from Benesi-Hildebrand plot using UV–vis and fluorescence spectrophotometer respectively. The detection limit of PPPC for Fe3+ was further determined as 57 nM and 88 nM by UV–vis and fluorescence titrations. Moreover, the binding mechanism of Fe3+ with PPPC was confirmed by DFT study.

MODULATORS OF OCULAR OXIDATIVE STRESS

Described herein are compounds, compositions and methods directed to the treatment of ophthalmic conditions characterized by oxidative stress or damage in a subject by reducing the reactive oxygen species in the subject. Also described herein are methods for reducing ophthalmic photooxidative damage in a subject.