502925-47-5

Usage

Uses

Used in Pharmaceutical Research:
6-(4-Methoxyphenyl)-2-pyridinecarboxaldehyde is used as a building block in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, 6-(4-Methoxyphenyl)-2-pyridinecarboxaldehyde is utilized as a key component in the creation of new agrochemicals, contributing to the development of effective solutions for pest control and crop protection.
Used in Organic Chemistry Reactions:
As a reagent in organic chemistry, 6-(4-Methoxyphenyl)-2-pyridinecarboxaldehyde plays a crucial role in facilitating various chemical reactions, enabling the synthesis of complex organic compounds.
Used in Anticancer Research:
6-(4-Methoxyphenyl)-2-pyridinecarboxaldehyde has been studied for its potential anticancer properties, showing promise in the development of new cancer treatments.
Used in Antifungal Applications:
6-(4-METHOXYPHENYL)-2-PYRIDINECARBOXALD& has also demonstrated antifungal properties, making it a candidate for use in the development of new antifungal agents to combat fungal infections.

InChI:InChI=1/C13H11NO2/c1-16-12-7-5-10(6-8-12)13-4-2-3-11(9-15)14-13/h2-9H,1H3

Upstream product

• 34160-40-2 6-bromo-2-pyridinecarbaldehyde 
• 5720-07-0 4-methoxyphenylboronic acid 

Downstream Products

• 1433897-52-9 C₆₈H₆₀N₈Ni₂O₄ 

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.

1-aryl-3-(6-arylpyridine-2-yl)-acrylketone, and preparation method and application thereof

The invention relates to 1-aryl-3-(6-arylpyridine-2-yl)-acrylketone. The molecular structure of the compound is shown in the following general formula: in the general formula, R1 is hydrogen or methoxy, R2 is hydrogen or methoxy, R3 is hydrogen or methoxy

Convenient and rapid strategies towards 6-(hetero)aryl pyridylmethylamines: First catalytic issues

The convenient preparation of new pyridylmethylamines is described using a short two step sequence. The first step involved the straightforward microwave-assisted construction of 6-aryl and 6-heteroaryl pyridine scaffolds bearing carboxaldehyde and nitrile fragments. The pendant arm comprising a second nitrogen atom by mean of amine and oxazoline moieties is installed in the second step. Finally, a first entry towards catalytic activity is given. In this context, modification of the ligand pattern and steric crowding around the central pyridine ring is examined and led to modest to fair ee's in the construction of binaphthyl substrates.

Biomimetic aryl hydroxylation derived from alkyl hydroperoxide at a nonheme iron center. Evidence for an FeIV=O oxidant

Many nonheme iron-dependent enzymes activate dioxygen to catalyze hydroxylations of arene substrates. Key features of this chemistry have been developed from complexes of a family of tetradentate tripodal ligands obtained by modification of tris(2-pyridyl