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Usage

Uses

Used in Pharmaceutical Synthesis:
2-(PYRIDIN-2-YLAMINOMETHYL)-PHENOL is used as a key intermediate in the synthesis of various pharmaceuticals. Its structural features allow for the development of new drugs with improved therapeutic properties and reduced side effects.
Used in Agrochemical Production:
In the agrochemical industry, 2-(PYRIDIN-2-YLAMINOMETHYL)-PHENOL serves as a building block for the creation of novel agrochemicals. Its incorporation into these compounds can enhance their effectiveness in pest control and crop protection.
Used in Organic Chemistry Research:
2-(PYRIDIN-2-YLAMINOMETHYL)-PHENOL is utilized as a versatile reagent in organic chemistry research. Its unique structure and reactivity make it a valuable component in the synthesis of new materials and compounds with potential applications in various industries.
Used in Antifungal Applications:
2-(PYRIDIN-2-YLAMINOMETHYL)-PHENOL has been studied for its potential antifungal properties. It can be used as an active ingredient in antifungal formulations to combat fungal infections in various settings, such as agriculture and medicine.
Used in Antioxidant Formulations:
Due to its antioxidant properties, 2-(PYRIDIN-2-YLAMINOMETHYL)-PHENOL can be incorporated into antioxidant formulations. These formulations can be used to protect materials from oxidative damage, extending their shelf life and improving their performance in various applications.

Upstream product

• 1823-47-8 2-(pyridine-2-yliminomethyl)phenol 
• 13563-04-7 N-(2'-pyridyl)-2-hydroxybenzamide 
• 504-29-0 2-aminopyridine 
• 90-02-8 salicylaldehyde 
• 17543-97-4 2-[(1E)-2-aza-2-(2-pyridyl)ethenyl]benzen-1-ol 

Downstream Products

• 949094-00-2 diacetato-bis(N-(2-hydroxybenzyl)-2-aminopyridine)copper(II) 

Relevant academic research and scientific papers

Convenient Assembly of Privileged (Hetero)Arene-Fused Benzo[1.4]oxazepines by Two Tandem SNAr Events. Part 2 – The Use of o-[N-(Hetero)aryl]aminomethyl Phenols

As was anticipated based on mechanistic reasoning, bis-nucleophilic o-(arylamino)methyl phenols underwent a facile, base-promoted cyclocondensation with reactivity matched bis-electrophilic (hetero)aromatic substrates to give a rare type of substituted di

A quick route for the synthesis of 3-Aryl-3,4-dihydro-2H-benz[e]-1,3- oxazin-2-ones

N-(2-Hydroxy)-benzyl-arylamines (1) gave substantially pure 3-aryl-3,4-dihydro-2H-benz[e]-1,3-oxazin-2-one 2 on cyclization with carbonyldiimidazole in DMSO in 20-30 min at 20-25 °C in excellent yields.

Synthesis and biological activity of some 3-aryl-3,4-dihydro-2h-benz[e]-1, 3-oxazines/6-bromo-3-aryl-3,4-dihydro-2h-benz[e]-1,3-oxazines

N-(2-Hydroxy)-benzyl-arylamine (1) gives substantially pure 3-aryl-3,4-dihydro-2H-benz[e]-1,3-oxazines/6-bromo-3-aryl-3,4-dihydro-2H-benz[e] -1,3-oxazines (2) on cyclization with formaldehyde in methanol within 0.5-1.0 h at 65-68 C in excellent yields. Th

Esters and Lactones of Phenolic Amino Carboxylic Acids: Prodrugs for Iron Chelation

The new iron chelator N,N'-bis(2-hydroxyphenyl)ethylenediamine-N,N'-diacetic acid (1), its dilactone 2, N,N'-bis(2-hydroxybenzyl)-2-hydroxypropylene-1,3-diamine-N,N'-diacetic acid (3), and its methyl ester lactone 4 and a series of esters of N,N'-bis(2-hy

Voltammetric studies of the electrochemical behaviour of salicylidene-2-aminopyridine at a hanging-mercury-drop-electrode

Electrochemical behaviour of salicylidene-2-aminopyridine has been investigated in 0.1M tetraethylammonium perchlorate - dimethylformamide solutions by cyclic voltammetric and convolution potential sweep voltammetric methods.It was found that the depolari

Electroreduction of Some Azomethine Compounds at Copper and Copper Amalgam Cathodes

The electrochemical reducibility of some azomethine compounds derived from aniline, its derivatives, 2-aminopyridine, and 2-aminobenzothiazole and aromatic aldehydes at copper and copper amalgam cathodes in acid medium has been investigated.It is found that reducibility of the compounds increases with increase in hydrogen overvoltage of the cathode and decrease in current density.Furthermore the reducibility of the azomethine compounds possessing non-hetero aromatic amine moiety is higher than that of compounds possessing heteroaromatic amine moiety.