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(E)-3-hydroxy-N′-(2-hydroxy-3-methoxybenzylidene)-2-naphthohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80648-85-7

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80648-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80648-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,4 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80648-85:
(7*8)+(6*0)+(5*6)+(4*4)+(3*8)+(2*8)+(1*5)=147
147 % 10 = 7
So 80648-85-7 is a valid CAS Registry Number.

80648-85-7Downstream Products

80648-85-7Relevant academic research and scientific papers

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

Bikas, Rahman,Lippolis, Vito,Noshiranzadeh, Nader,Farzaneh-Bonab, Hossein,Blake, Alexander J.,Siczek, Milosz,Hosseini-Monfared, Hassan,Lis, Tadeusz

, p. 999 - 1006 (2017/02/23)

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

Structure-activity relationships in non-ligand binding pocket (Non-LBP) diarylhydrazide antiandrogens

Caboni, Laura,Egan, Billy,Kelly, Brendan,Blanco, Fernando,Fayne, Darren,Meegan, Mary J.,Lloyd, David G.

, p. 2116 - 2130 (2013/09/23)

We report the synthesis and a study of the structure-activity relationships of a new series of diarylhydrazides as potential selective non-ligand binding pocket androgen receptor antagonists. Their biological activity as antiandrogens in the context of the development of treatments for castration resistant prostate cancer was evaluated using in vitro time resolved fluorescence resonance energy transfer and fluorescence polarization on target assays. Additionally, a theoretical study combining docking and molecular dynamics methods was performed to provide insight into their mechanism of action as a basis for further lead optimization studies.

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

Monfared, Hassan Hosseini,Bikas, Rahman,Mayer, Peter

experimental part, p. 2574 - 2583 (2011/02/17)

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.

COMPLEXES OF Co(II), Ni(II) AND Zn(II) WITH 3-HYDROXY-2-NAPHTHOYL HYDRAZONES OF SOME AROMATIC ALDEHYDES

Osman, M. M.,Ali, G. Y.

, p. 13 - 24 (2007/10/02)

3-Hydroxy-2-naphthoyl hydrazones of benzaldehyde, p-chlorobenzaldehyde, p-nitrobenzaldehyde, vaniline, o-vaniline and salicylaldehyde together with their metal complexes have been prepared.All compounds have been characterized by chemical analysis and i.r

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