1149-69-5

Usage

Uses

Used in Chemical Synthesis:
1-(4-Methoxybenzylidene)-2-benzylidenehydrazine is used as a precursor in the chemical synthesis of heterocyclic compounds for its unique molecular structure and reactivity.
Used in Corrosion Inhibition:
1-(4-Methoxybenzylidene)-2-benzylidenehydrazine is used as a corrosion inhibitor in various industries, such as the automotive and aerospace industries, to protect metal surfaces from degradation and extend the lifespan of equipment.
Used in Pharmaceutical Research:
1-(4-Methoxybenzylidene)-2-benzylidenehydrazine is used as a compound of interest in pharmaceutical research for its potential anti-tubercular and anti-cancer properties, aiming to develop new drugs for the treatment of tuberculosis and various types of cancer.
Used in Material Science:
1-(4-Methoxybenzylidene)-2-benzylidenehydrazine is used in material science for its potential applications in the development of new materials with specific properties, such as improved stability or reactivity, due to its unique chemical structure.

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 1574-10-3 benzaldehyde semicarbazone 
• 100-51-6 benzyl alcohol 
• 105-13-5 4-Methoxybenzyl alcohol 
• 4334-74-1 4-methoxybenzylidene thiosemicarbazone 
• 100-52-7 benzaldehyde 
• 2700-22-3 Benzylidenemalononitrile 
• 2025-40-3 ethyl benzylidenecyanoacetate 
• 824-94-2 p-methoxybenzyl chloride 
• 140-69-2 4-methoxybenzylhydrazine 
• 100-44-7 benzyl chloride 
• 555-96-4 Benzylhydrazine 

Relevant academic research and scientific papers

Azines from one-pot reaction of thiosemicarbazones

Thermolysis and/or microwave irradiation of thiosemicarbazones gave the corresponding isothiocyanates, which on addition of either activated nitriles or aldehydes furnished various types of azines. The mechanism was discussed. The structures of products were proved by MS, IR, NMR, and elemental analyses (Image presented).

Novel synthesis of unsymmetrical azines from semicarbazones and aldehydes

A new synthesis of unsymmetrical azines utilizing semicarbazones and aldehyde is described.

Oxidized multiwalled nanotubes as efficient carbocatalyst for the general synthesis of azines

The carbocatalytic synthesis of azines (N-N linked diimines) by mild-oxidized multiwalled carbon nanotubes catalyst (oxMWNT) is presented. The material, just with a 5 %wt. loading, is able to carry out a smooth room-temperature metal-free condensation of

Metal-Free Synthesis of 1,3,4-Oxadiazoles from N′-(Arylmethyl)hydrazides or 1-(Arylmethyl)-2-(arylmethylene)hydrazines

An efficient and versatile metal-free synthesis of 1,3,4-oxadiazoles from N′-(arylmethyl)hydrazides or 1-(arylmethyl)-2-(arylmethylene)hydrazines through oxidative dehydrogenation is reported. A range of 2,5-disubstituted 1,3,4-oxadiazoles were prepared by treating N′-(arylmethyl)hydrazides with (diacetoxyiodo)benzene in acetonitrile or by treating 1-(arylmethyl)-2-(arylmethylene)hydrazines with [bis(trifluoroacetoxy)iodo]benzene in methyl tert-butyl ether. Aldehyde N-acylhydrazones and aldazines were initially generated in situ as intermediates.