21883-34-1

Usage

Uses

Used in Organic Synthesis:
2-(diphenylmethyl)pyridine 1-oxide is utilized as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-(diphenylmethyl)pyridine 1-oxide serves as an intermediate in the production of drugs, playing a crucial role in the synthesis of active pharmaceutical ingredients.
Used in Agrochemical Production:
Similarly, in agrochemical manufacturing, 2-(diphenylmethyl)pyridine 1-oxide is employed as an intermediate, aiding in the synthesis of compounds that protect crops from pests and diseases.
Used in Antimicrobial Applications:
2-(diphenylmethyl)pyridine 1-oxide is studied for its potential as an antimicrobial agent, given its ability to inhibit the growth of certain microorganisms, which could be beneficial in various medical and industrial settings.
Used in Antiprotozoal Applications:
2-(diphenylmethyl)pyridine 1-oxide is also being investigated for its antiprotozoal properties, indicating its potential use in treating infections caused by protozoan parasites, which can be significant in both human and veterinary medicine.

Upstream product

• 3678-70-4 Diphenyl-2-pyridylmethan 
• 110-86-1 pyridine 
• 694-59-7 pyridine N-oxide 
• 4545-20-4 benzophenone tosylhydrazone 

Downstream Products

• 2417528-06-2 (R)-2-(6-benzhydrylpyridin-2-yl)-4-phenyl-4,5-dihydrooxazole 
• 2417528-09-5 C₃₃H₂₆N₂O 

Relevant academic research and scientific papers

Switchable Oxidative Reactions of N-allyl-2-Aminophenols: Palladium-Catalyzed Alkoxyacyloxylation vs an Intramolecular Diels-Alder Reaction

The Pd(II)-catalyzed reaction of N-allyl-2-aminophenols in the presence of PhI(OCOR)2 as the oxidant resulted in an alkoxyacyloxylation process, with the formation of functionalized dihydro-1,4-benzoxazines. The reaction performed in the absence of pallad

Palladium(II)-Catalyzed Enantioselective Azidation of Unactivated Alkenes

The first Pd-catalyzed enantioselective azidation of unactivated alkenes has been established by using readily accessible 1-azido-1,2-benziodoxol-3(1H)-one (ABX) as an azidating reagent, which affords a wide variety of structurally diverse 3-N3

Enantioselective Pd(II)-Catalyzed Intramolecular Oxidative 6- endo Aminoacetoxylation of Unactivated Alkenes

A novel asymmetric 6-endo aminoacetoxylation of unactivated alkenes by palladium catalysis, which yields chiral β-acetoxylated piperidines with excellent chemo-, regio- and enantioselectivities under very mild reaction conditions, has been established herein by employing a new designed pyridine-oxazoline (Pyox) ligand. Importantly, introducing a sterically bulky group into the C-6 position of Pyox is crucial to enhance the reactivity of the aminoacetoxylation of alkenes.

The microwave-assisted ortho-alkylation of azine N-oxides with N-tosylhydrazones catalyzed by copper(i) iodide

A copper catalyzed regioselective cross-coupling of N-tosylhydrazones with azine N-oxides to yield ortho-alkylated products in moderate to good yields is reported. The reaction is facilitated by microwave, takes place without any ligand, and uses inexpensive copper(i) iodide as the catalyst.