356058-14-5

Usage

Uses

Used in Organic Synthesis:
6-(4-TRIFLUOROMETHYL-PHENYL)-PYRIDINE-3-CARBALDEHYDE is used as a key intermediate in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of complex molecular structures.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-(4-TRIFLUOROMETHYL-PHENYL)-PYRIDINE-3-CARBALDEHYDE is utilized as a building block for the preparation of drugs. Its trifluoromethyl-phenyl group can impart specific bioactivity or physicochemical properties to the resulting molecules, which is crucial in drug discovery and development.
Used in Agrochemical Industry:
6-(4-TRIFLUOROMETHYL-PHENYL)-PYRIDINE-3-CARBALDEHYDE also serves as a valuable component in the agrochemical sector, where it is used in the synthesis of compounds with pesticidal or herbicidal properties, enhancing the effectiveness of these products.
Used in Materials Science:
In the field of materials science, 6-(4-TRIFLUOROMETHYL-PHENYL)-PYRIDINE-3-CARBALDEHYDE is employed for its potential to contribute to the development of new materials with tailored properties, such as improved stability or specific interactions with other molecules.

Upstream product

• 149806-06-4 6-bromonicotinaldehyde 
• 214360-65-3 4-trifluoromethylphenylboronic acid pinacol ester 
• 356058-34-9 methyl 6-(4-(trifluoromethyl)phenyl)nicotinate 
• 356058-13-4 5-hydroxymethyl-2-(4-trifluoromethylphenyl)pyridine 
• 128796-39-4 4-trifluoromethylphenylboronic acid 

Downstream Products

• 356058-13-4 5-hydroxymethyl-2-(4-trifluoromethylphenyl)pyridine 
• 871250-36-1 1-(6-(4-(trifluoromethyl)phenyl)pyridin-3-yl)propan-1-ol 
• 871251-14-8 (R,S)-(4-tert-butyl-phenyl)-[6-(4-trifluoromethyl-phenyl)-pyridin-3-yl]-methanol 
• 203065-88-7 2-(4-trifluoromethylphenyl)pyridine 
• 1361968-52-6 1-(6-(4-(trifluoromethoxy)phenyl)pyridin-3-yl)propan-1-one 
• 1361967-36-3 C₂₂H₁₅F₃N₂O 

Relevant academic research and scientific papers

Metal-Free Aerobic Oxidative Selective C-C Bond Cleavage in Heteroaryl-Containing Primary and Secondary Alcohols

A transition-metal-free aerobic oxidative selective C-C bond-cleavage reaction in primary and secondary heteroaryl alcohols is reported. This reaction was highly efficient and tolerated various heteroaryl alcohols, generating a carboxylic acid derivative and a neutral heteroaromatic compound. Experimental studies combined with density functional theory calculations revealed the mechanism underlying the selective C-C bond cleavage. This strategy also provides an alternative simple approach to carboxylation reaction.

Carboxylic acid derivatives and preparation method and use in medicines thereof

The invention relates to carboxylic acid derivatives and a preparation method and use in medicines thereof. Specifically, the invention relates to carboxylic acid derivatives as shown in the general formula (I), a preparation method and pharmaceutically a

Identification, design and biological evaluation of heterocyclic quinolones targeting plasmodium falciparum Type II NADH:Quinone oxidoreductase (PfNDH2)

Following a program undertaken to identify hit compounds against NADH:ubiquinone oxidoreductase (PfNDH2), a novel enzyme target within the malaria parasite Plasmodium falciparum, hit to lead optimization led to identification of CK-2-68, a molecule suitab

BENZOAZEPIN-OXY-ACETIC ACID DERIVATIVES AS PPAR-DELTA AGONISTS USED FOR THE INCREASE OF HDL-C, LOWER LDL-C AND LOWER CHOLESTEROL

The invention is directed to compounds of Formula (I) useful as PPAR agonists. Pharmaceutical compositions and methods of treating one or more conditions including, but not limited to, diabetes, nephropathy, neuropathy, retinopathy, polycystic ovary syndr

Pyrimidinone compounds

Pyrimidinone compounds of formula (I) are inhibitors of the enzyme Lp-PLA2 and of use in therapy, in particular for treating atherosclerosis.