81259-54-3

Usage

Uses

Used in Pharmaceutical Industry:
4-(Benzyloxy)-3-methoxybenzaldehyde oxime is used as a key intermediate in the synthesis of pharmaceuticals for its reactivity and the presence of functional groups that facilitate the creation of complex molecular structures.
Used in Chemical Industry:
In the chemical industry, 4-(Benzyloxy)-3-methoxybenzaldehyde oxime serves as a versatile reagent in various organic reactions, contributing to the development of new organic compounds and materials.

InChI:InChI=1/C15H15NO3/c1-18-15-9-13(10-16-17)7-8-14(15)19-11-12-5-3-2-4-6-12/h2-10,17H,11H2,1H3/b16-10-

Upstream product

• 2426-87-1 3-methoxy-4-(phenylmethoxy)benzaldehyde 
• 121-33-5 vanillin 
• 2874-33-1 vanillin oxime 
• 100-39-0 benzyl bromide 

Downstream Products

• 2426-87-1 3-methoxy-4-(phenylmethoxy)benzaldehyde 
• 130972-89-3 (4-hydroxy-3-methoxybenzyl)carbamic acid tert-butyl ester 
• 388570-41-0 5-cyane-3-[(4-phenylmethoxy-3-methoxy)-phenyl]-4,5-dihydroisoxazole 

Relevant academic research and scientific papers

Solvent free, microwave assisted conversion of aldehydes into nitriles and oximes in the presence of NH2OH · HCl and TiO2

Aromatic aldehydes bearing electron-donating groups are easily converted into their respective nitriles using NH2OH · HCl and TiO 2 under microwave irradiation, while those bearing an electron-withdrawing group give the corresponding oximes.

An efficient chemoselective etherification of phenols in polyfunctional aromatic compounds

A simple and efficient chemoselective alkylation of phenols in polyfunctional aromatic compounds with different alkyl halides in the presence of K2CO3/TBAB is reported. The method is successful with various hydroxy aromatic acids or oximes possessing other functional groups.

Synthesis of new 4,5-dihydroisoxazoles with potential anti-inflammatory activity

This paper reports the synthesis of different 4,5-dihydroisoxazoles which may present anti-inflammatory activity. The methodology employed was based on the 1,3-dipolar cycloaddition of nitrile oxide derived from vanillin to unsaturated compounds. It was u

A new one pot method for the conversion of aldehydes into nitriles using hydroxyamine and phthalic anhydride

The aryl and alkyl aldehydes were readily converted to give the corresponding nitrites in good yields using hydroxyamine and phthalic anhydride as reagents in one pot.