80648-85-7

Basic information

• Product Name: (E)-3-hydroxy-N′-(2-hydroxy-3-methoxybenzylidene)-2-naphthohydrazide
• Synonyms: (E)-3-hydroxy-N′-(2-hydroxy-3-methoxybenzylidene)-2-naphthohydrazide
• CAS NO: 80648-85-7
• Molecular Weight: 336.347
• Mol File: 80648-85-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (E)-3-hydroxy-N′-(2-hydroxy-3-methoxybenzylidene)-2-naphthohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-hydroxy-N′-(2-hydroxy-3-methoxybenzylidene)-2-naphthohydrazide(80648-85-7)
• EPA Substance Registry System: (E)-3-hydroxy-N′-(2-hydroxy-3-methoxybenzylidene)-2-naphthohydrazide(80648-85-7)

Safety Data

• Hazardous Substances Data: 80648-85-7(Hazardous Substances Data)

Upstream product

• 5341-58-2 3-hydroxy-2-naphthohydrazide 
• 148-53-8 3-methoxy-2-hydroxybenzaldehyde 
• 883-99-8 3-hydroxy-2-naphthoic acid methyl ester 
• 92-70-6 3-Hydroxy-2-naphthoic acid 

Relevant articles and documents

Electronic Effects of Aromatic Rings on the Catalytic Activity of Dioxidomolybdenum(VI)–Hydrazone Complexes

Nine dioxidomolybdenum(VI) complexes were synthesized through the reactions of MoO3with tridentate hydrazone Schiff base ligands obtained from the reactions of aromatic acid hydrazides (3-hydroxy-2-naphthoic acid hydrazide, 4-pyridinecarboxylic

Homogeneous green catalysts for olefin oxidation by mono oxovanadium(V) complexes of hydrazone Schiff base ligands

Three mono oxovanadium(V) complexes of tridentate Schiff base ligands [VO(OMe)L'] (1), [VO(OMe)L2] (2) and [VO(OMe)L3] (3) obtained by monocondensation of 3-hydroxy-2-naphthohydrazide and aromatic o-hydroxyaldehydes have been synthesized (H2L2 - (E)-3-hydroxy-N′-(2-hydroxy-3-methoxybenzylidene)-2-naphthohydrazide, H2L2 - (E)-3-hydroxy-N′-(2-hydroxybenzylidene)-2- naphthohydrazide and H2L3 - (E)-N′-(5-bromo-2- hydroxybenzylidene)-3-hydroxy-2-naphthohydrazide). The complexes were characterized by spectroscopic methods in the solid state (IR) and in solution (UV-Vis, 1H NMR). Single crystal X-ray analyses were performed with 1 and 2. The catalytic potential of these complexes has been tested for the oxidation of cyclooctene using H2O2 as the terminal oxidant. The effects of various parameters including the molar ratio of oxidant to substrate, the temperature, and the solvent have been studied. The catalyst 2 showed the most powerful catalytic activity in oxidation of various terminal, cyclic and phenyl substituted olefins. Excellent conversions have been obtained for the oxidation of cyclic and bicyclic olefins.