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(E)-N′-(2-hydroxybenzylidene)-2-phenylacetohydrazide is a chemical compound with the molecular formula C15H13N2O2. It is an organic compound that belongs to the class of hydrazides, specifically a derivative of acetohydrazide. (E)-N′-(2-hydroxybenzylidene)-2-phenylacetohydrazide is characterized by a phenyl group attached to the acetohydrazide moiety, with a 2-hydroxybenzylidene group forming a double bond with the nitrogen atom. The "E" configuration indicates the geometric isomerism of the double bond, where the phenyl and hydroxybenzyl groups are on opposite sides of the double bond. (E)-N′-(2-hydroxybenzylidene)-2-phenylacetohydrazide may have potential applications in pharmaceuticals or as an intermediate in the synthesis of other organic compounds due to its unique structure and reactivity.

4830-84-6

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4830-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4830-84-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,3 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4830-84:
(6*4)+(5*8)+(4*3)+(3*0)+(2*8)+(1*4)=96
96 % 10 = 6
So 4830-84-6 is a valid CAS Registry Number.

4830-84-6Downstream Products

4830-84-6Relevant academic research and scientific papers

Spectroscopic, density functional theory, nonlinear optical properties and in vitro biological studies of Co(II), Ni(II), and Cu(II) complexes of hydrazide Schiff base derivatives

Ramadan, Ramadan M.,El-Medani, Samir M.,Makhlouf, Abdelmoneim,Moustafa, Hussein,Afifi, Manal A.,Haukka, Matti,Abdel Aziz, Ayman

, (2021)

Complexes of three molecularly designed phenylacetohydrazide Schiff base derivatives—N′-(2-hydroxybenzylidene)-2-phenylacetohydrazid (HL1), N-(1-(2-hydroxyphenyl)ethylidene)-2-phenylacetohydrazide (HL2), and N′-((1-hydroxynaphthalen-2-yl)methylene)-2-phenylacetohydrazide (HL3)—with some bivalent metal ions were synthesized and investigated by several spectroscopic and analytical techniques. The crystal structure of HL1 ligand has been solved by conventional X-ray diffraction technique. Molecular geometries of HL1 and the studied complexes were investigated using the DFT-B3LYP/GENECP level of theory. Quantum and non-quantum global reactivity descriptors as well as the nonlinear optical properties were calculated. Biological parameters such as antimicrobial and antioxidant activities, fluorescence quenching studies, and viscosity measurements of the complexes were carried out. Molecular docking studies of HL1 and complexes using Molecular Operating Environment (MOE) software are reported. The different biological studies and the molecular docking were correlated to each other. The biological studies supported that the complexes can bind to DNA via intercalative mode and showed a various DNA binding potency.

Influence of synthesis conditions on complexation of Cu (II) with O,N,O tridentate hydrazone ligand. X-ray diffraction and spectroscopic investigations

Repich,Orysyk,Orysyk,Zborovskii, Yu.L.,Melnyk,Trachevskyi,Pekhnyo,Vovk

, p. 222 - 232 (2017)

Four novel Cu2+ coordination compounds with a (E)-N′-(2-hydroxybenzylidene)-2-phenylacetohydrazide (HBPAH, H2L) have been synthesized and characterized by single crystal X-ray diffraction method, IR, UV–Vis and EPR spectroscopy. In a

Design, synthesis and in vitro antimalarial activity of an acylhydrazone library

Melnyk, Patricia,Leroux, Virginie,Sergheraert, Christian,Grellier, Philippe

, p. 31 - 35 (2007/10/03)

A library of acylhydrazone iron chelators was synthesized and tested for its ability to inhibit the growth of a chloroquine-resistant strain of Plasmodium falciparum. Some of these new compounds are significantly more active than desferrioxamine DFO, the

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