5880-63-7

Usage

InChI:InChI=1/C14H13N3O3/c1-20-14-8-2-11(3-9-14)10-15-16-12-4-6-13(7-5-12)17(18)19/h2-10,16H,1H3

Upstream product

• 64-17-5 ethanol 
• 4180-23-8 E-1-(4'-methoxyphenyl)prop-1-ene 
• 104-46-1 anethole 
• 64-19-7 acetic acid 
• 123-11-5 4-methoxy-benzaldehyde 
• 100-16-3 4-nitrophenylhydrazone 
• 539-12-8 4-Propenyl-phenol 
• 77-78-1 dimethyl sulfate 
• 3155-23-5 4-hydroxy-benzaldehyde-(4-nitro-phenylhydrazone) 
• 186581-53-3 diazomethane 
• 60-29-7 diethyl ether 

Downstream Products

• 123-11-5 4-methoxy-benzaldehyde 
• 52778-19-5 C₂₆H₂₂N₄O₃S₂ 
• 100-09-4 4-methoxybenzoic acid 
• 1370004-51-5 C₁₈H₁₈N₄O₃ 
• 1370004-52-6 C₁₇H₁₆N₄O₃ 
• 17355-71-4 3-(4-methoxy-phenyl)-1-(4-nitro-phenyl)-5-phenyl-1H-[1,2,4]triazole 
• 1186197-21-6 C₂₆H₂₂N₃O₃P 
• 52778-20-8 C₂₀H₁₆N₄O₃S 
• 79650-56-9 4-Methoxy-benzoic acid N'-acetyl-N'-(4-nitro-phenyl)-hydrazide 
• 78893-10-4 1-p-nitrophenyl-3-anisyl-s-triazolo<4,3-a>pyridinium perchlorate 

Relevant academic research and scientific papers

Synthesis, crystal structure, optical and electrochemical properties of novel diphenylether-based formazan derivatives

In this study, formazans 5a-5h were synthesized by coupling the reactions of substituted phenylhydrazone compounds 3a-3h with diazonium salt of 4-chloro-2-phenoxybenzenamine (4). The substituted phenylhydrazones 3a-3h were obtained from the condensation o

Modification of fulleropyrazolines modulates their cleavage by light

The extraordinary electrochemistry and the tunability of their energy levels allows the use of fulleropyrazolines in photovoltaics and charge-transfer systems. Here we show that substitution in position 1 tunes photolytic stability; electron-donating groups facilitate 1,3-dipolar cycloreversion to fullerene. This discovery has implications not only for photovoltaic stability but also highlights a potential strategy for photo-controlled fullerene release systems ('photo-caged'/'photo-activated' fullerene). This journal is

Ultrasound assisted syntheses of some 1,2,4-triazole derivatives

A facile preparation of a series of 1,2,4-triazole derivatives under ultrasound irradiation, that proceeded via one-pot reaction of a- nitrophenyl hydrazones with different methylene amines, using sodium nitrite as oxidant and benzyl triethyl ammonium chloride (BTEAC) as phase transfer catalysis, respectively, was described.

Arylaldehydes-pentafluorophenyl hydrazones as second-order nonlinear optical chromophores: A novel approach for remarkably defeating the nonlinearity-transparency trade-off

A series of new arylhydrazone chromophores containing pentafluorophenyl as electronic acceptor are synthesized and found to exhibit significantly blue-shifted absorption in comparison with the corresponding 4-nitrophenyl analogues while keeping β value in