22123-19-9

Usage

Uses

Used in Pharmaceutical Applications:
6-METHYL-4-(TRIFLUOROMETHYL)-2(1H)-PYRIDONE is used as a building block for the synthesis of bioactive molecules, contributing to the development of new pharmaceutical compounds. Its unique chemical structure allows for the creation of drugs with specific therapeutic properties.
Used in Agrochemical Applications:
In the agrochemical industry, 6-METHYL-4-(TRIFLUOROMETHYL)-2(1H)-PYRIDONE is utilized as a precursor in the synthesis of agrochemicals, potentially leading to the development of new pesticides or herbicides with improved efficacy and selectivity.
Used in Materials Science:
6-METHYL-4-(TRIFLUOROMETHYL)-2(1H)-PYRIDONE is employed in materials science for its potential to contribute to the development of new materials with unique properties, such as enhanced stability or specific interactions with other molecules.
Used as a Reagent in Organic Synthesis:
As a reagent in organic synthesis, 6-METHYL-4-(TRIFLUOROMETHYL)-2(1H)-PYRIDONE is used to facilitate various chemical reactions, enabling the synthesis of a wide range of organic compounds for research and industrial applications.

InChI:InChI=1/C7H6F3NO/c1-4-2-5(7(8,9)10)3-6(12)11-4/h2-3H,1H3,(H,11,12)

Upstream product

• 654-49-9 6-methyl-2-oxo-4-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile 
• 367-57-7 1,1,1-Trifluoro-2,4-pentanedione 

Downstream Products

• 451459-17-9 2-bromo-6-methyl-4-(trifluoromethyl)pyridine 

Relevant academic research and scientific papers

Remote sp2C-H Carboxylation via Catalytic 1,4-Ni Migration with CO2

A remote catalytic reductive sp2 C-H carboxylation of arenes with CO2 (1 bar) via 1,4-Ni migration is disclosed. This protocol constitutes the first catalytic 1,4-Ni migration reported to date, thus offering new vistas in the Ni-catalyzed reductive coupling arena while providing an unconventional new platform for incorporating electrophilic sites at remote sp2 C-H linkages.

Design, synthesis and biological evaluation of benzimidazole-pyridine-piperidine hybrids as a new class of potent antimicrobial agents

A series of novel benzimidazole-pyridine-piperidine hybrids was synthesized in good yields and characterized by spectral and elemental analyses. The compounds 4a-h and 5a-c were evaluated for their in vitro antibacterial activity against gram-positive org

4,4′-Bis(trifluoromethyl)-2,2′-bipyridine-a multipurpose ligand scaffold for lanthanoid-based luminescence/19F NMR probes

The tetradentate ligand 4,4′-bis(trifluoromethyl)-2,2′- bipyridine-6,6′-dicarboxylic acid (H21) and three corresponding anionic rare earth complexes [RE(1)2]- (RE = Y, Tb, Dy) were synthesized. The terbium and dysprosium complexes show lanthanoid-centered luminescence in aqueous solution, as well as paramagnetically enhanced longitudinal magnetic relaxation of the 19F nuclei.