80714-39-2

Usage

Uses

Used in Chemical Synthesis:
2(1H)-Pyridinone,6-fluoro-,hydrazone(9CI) is used as a synthetic intermediate for the preparation of various organic compounds. Its hydrazone functional group allows for versatile reactions, such as condensation, cyclization, and reduction, enabling the synthesis of a wide range of chemical products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2(1H)-Pyridinone,6-fluoro-,hydrazone(9CI) serves as a key building block for the development of novel drug candidates. Its hydrazone moiety can be utilized to design and synthesize bioactive molecules with potential therapeutic applications. 2(1H)-Pyridinone,6-fluoro-,hydrazone(9CI)'s ability to form stable complexes with metal ions also makes it a promising candidate for the development of metal-based drugs.
Used in Biological Activity Studies:
2(1H)-Pyridinone,6-fluoro-,hydrazone(9CI) is used as a research tool to investigate its potential biological activities. Due to its hydrazone functional group, the compound may exhibit various biological effects, such as antioxidant, antimicrobial, or anti-inflammatory properties. These activities can be explored in different biological systems, providing valuable insights into the compound's therapeutic potential.
Used in Analytical Chemistry:
In analytical chemistry, 2(1H)-Pyridinone,6-fluoro-,hydrazone(9CI) can be employed as a reagent or a ligand in the development of analytical methods for the detection and quantification of various analytes. Its ability to form complexes with metal ions can be utilized in the design of colorimetric, fluorometric, or electrochemical sensors for the selective and sensitive detection of target molecules.

Upstream product

• 626-05-1 2,6-Dibromopyridine 
• 1513-65-1 2,6-difluoro pyridine 
• 20885-12-5 2-chloro-6-fluoropyridine 

Downstream Products

• 1431142-67-4 C₂₆H₂₁Cl₂F₄N₇O₂ 
• 1427301-05-0 C₂₁H₁₃Cl₂F₄N₇ 
• 75771-87-8 2-(6-fluoro-2-pyridinyl)hydrazinecarboxamide 

Relevant academic research and scientific papers

Triazolo and imidazo dihydropyrazolopyrimidine potassium channel antagonists

Previously disclosed C6 amido and benzimidazole dihydropyrazolopyrimidines were potent and selective blockers of IKur current. Syntheses and SAR for C6 triazolo and imidazo dihydropyrazolopyrimidines series are described. Trifluoromethylcyclohexyl N(1) triazole, compound 51, was identified as a potent and selective Kv1.5 inhibitor with an acceptable PK and liability profile.

COMPOUNDS FOR FLUORESCENCE LABELING

There are provided fluorescent compounds that can be used for DNA sequencing, measurement of physiologically active substance or the like based on fluorescence immunoassay and so forth. Compounds represented by the formula (I) (V1 to V5 represent a hydrogen atom or a functional group selected from the group consisting of a halogen atom, an alkyl group, an alkenyl group, a group that can form a covalent bond with a compound to be labeled and the like, and V1, V2 and others may bind to each other to form a saturated or unsaturated ring; R1 represents a hydrogen atom or a functional group selected from the group consisting of an alkyl group, an aryl group and a heterocyclic group; R3 and R4 represent an alkyl group, and R3 and R4 may bind to each other to form a ring; Q represents a group of atoms required to form a methine dye chromophore; and m and n represent 0 or 1, provided that m + n is 1) or salts thereof.

Novel (1H-1,2,3-triazol-1-yl)pyridines

Pyridine ring substituted (1H-1,2,3-triazol-1-yl)pyridines were prepared and found to have insecticidal utility. 2-Chloro-6-(1H-1,2,3-triazol-1-yl)pyridine, for example, was prepared from 2-azio-6-chloropyridine and methyl propiolate by sequential condensation, hydrolysis, and decarboxylation and found to control aster leafhoppers.