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2-hydroxy-1-naphthalaldehyde salicyloylhydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54009-54-0

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54009-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54009-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,0 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54009-54:
(7*5)+(6*4)+(5*0)+(4*0)+(3*9)+(2*5)+(1*4)=100
100 % 10 = 0
So 54009-54-0 is a valid CAS Registry Number.

54009-54-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-N'-[(Z)-(2-oxonaphthalen-1-ylidene)methyl]benzohydrazide

1.2 Other means of identification

Product number -
Other names 5,6-benzosalicylidene-salicyloyl hydrazide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54009-54-0 SDS

54009-54-0Downstream Products

54009-54-0Relevant academic research and scientific papers

Fluorescence modulation of naphthalene containing salicyl hydrazide-based receptor through aggregation-induced emission enhancement approach: Dual detection of lanthanum and cyanide ions in semi-aqueous medium

Joshi, Pooja,Ali, Shah Raj,Rishu,Bhardwaj, Vimal K.

, p. 986 - 994 (2021)

The sensing activity of naphthalene containing salicyl hydrazide-based fluorescence receptor has been improved through aggregation-induced enhanced emission mechanism approach in semi-aqueous medium. The receptor has been found to be selective toward Las

A pH tuning single fluorescent probe based on naphthalene for dual-analytes (Mg2+and Al3+) and its application in cell imaging

Cui, Shuhua,Ji, Yuxiang,Jian, Li,Wen, Shaobai,Yu, Chunwei,Zhang, Jun

, p. 21399 - 21405 (2020)

In this study, a naphthalene Schiff-basePwhich serves as a dual-analyte probe for the quantitative detection of Al3+and Mg2+has been designed. The proposed probe showed an ‘‘off-on’’ fluorescent response toward Al3+in etha

Spectrofluorimetric determination of hydrogen peroxide with 2-hydroxy-1-naphthaldehyde salicyloylhydrazone (HNSH) as the substrate for horseradish peroxidase (HRP)

Tang,Wang,Sun,Xi Shen

, p. 141 - 148 (2002)

The oxidation reaction of HNSH with H2O2 under the catalysis of HRP was studied in detail. The possible reaction mechanism was discussed. Under optimum experimental conditions, the oxidized product of HNSH had excitation and emission

Versatile Reactivity and Theoretical Evaluation of Mono- and Dinuclear Oxidovanadium(V) Compounds of Aroylazines: Electrogeneration of Mixed-Valence Divanadium(IV,V) Complexes

Dash, Subhashree P.,Roy, Satabdi,Mohanty, Monalisa,Carvalho, M. Fernanda N. N.,Kuznetsov, Maxim L.,Pessoa, Jo?o Costa,Kumar, Amit,Patil, Yogesh P.,Crochet, Aurélien,Dinda, Rupam

, p. 8407 - 8421 (2016)

The substituted hydrazones H2L1-4 (L1-4 = dibasic tridentate ONO2- donor ligands) obtained by the condensation of 2-hydroxy-1-naphthaldehyde and 2-aminobenzoylhydrazine (H2hnal-abhz) (H2Ls

New molybdenum (VI) catalyst for the epoxidation of alkenes and oxidation of sulfides: An experimental and theoretical study

Bagherzadeh, Mojtaba,Haghdoost, Mohammad Mehdi,Ghanbarpour, Alireza,Amini, Mojtaba,Khavasi, Hamid Reza,Payab, Ebrahim,Ellern, Arkady,Woo, L. Keith

, p. 61 - 66 (2014)

The preparation and catalytic activity of molybdenum(VI) dioxido complex [MoO2L(C2H5OH)] (L = N′-[1-(2- hydroxynaphthyl)ethylidene]-2-hydroxy benzohydrazide) are reported. The reaction of the respective benzohydrazide liga

Benzoyl hydrazine derivative P and synthesis and application thereof

-

Paragraph 0021-0023, (2018/03/23)

The invention relates to detection of a fluorescence method on metal ions, and particularly relates to a benzoyl hydrazine derivative P which identifies and detects two different metal ions Mg andAl separately in different pH conditions. The structural formula of the benzoyl hydrazine derivative P is as shown in a formula (1). The preparation method of the benzoyl hydrazine derivative P comprises the following steps: firstly, carrying out hydrazinolysis on ethyl salicylate; carrying out a reaction with o-hydroxy naphthaldehyde at a molar ratio of 1 to 1 for 4 hours at 80 DEG C in anhydrous ethanol; cooling the mixture and separating out a solid and carrying out suction filtration; washing the mixture with a lot of water and anhydrous ethanol successively; and drying the solid to obtain a light yellow solid pure product P. The benzoyl hydrazine derivative P can be used for detecting Mg and Al separately in different pH conditions as a fluorescent probe. The benzoyl hydrazine derivative P is obtained by means of an effective synthetic means and shows relatively good selectivity on the metal ions Mg and Al separately. On a basis of an optimized experimental condition, the metal ions Mg and Al can be detected separately. The formula is as show in the description.

Synthesis, structural studies and catalytic activity of dioxidomolybdenum(VI) complexes with aroylhydrazones of naphthol-derivative

Pasayat, Sagarika,Dash, Subhashree P.,Roy, Satabdi,Dinda, Rupam,Dhaka, Sarita,Maurya, Mannar R.,Kaminsky, Werner,Patil, Yogesh P.,Nethaji

, p. 1 - 10 (2013/10/08)

Reaction of the salicylhydrazone of 2-hydroxy-1-naphthaldehyde (H 2L1), anthranylhydrazone of 2-hydroxy-1-naphthaldehyde (H2L2), benzoylhydrazone of 2-hydroxy-1-acetonaphthone (H2L3) and anthranylhydrazone of 2-hydroxy-1- acetonaphthone (H2L4; general abbreviation H2L) with [MoO2(acac)2] afforded a series of 5- and 6- coordinate Mo(VI) complexes of the type [MoO2L1-2(ROH)] [where R = C2H5 (1) and CH3 (2)], and [MoO 2L3-4] (3 and 4). The substrate binding capacity of 1 has been demonstrated by the formation of one mononuclear mixed-ligand dioxidomolybdenum complex [MoO2L1(Q)] {where Q = γ-picoline (1a)}. Molecular structure of all the complexes (1, 1a, 2, 3 and 4) is determined by X-ray crystallography, demonstrating the dibasic tridentate behavior of ligands. All the complexes show two irreversible reductive responses within the potential window -0.73 to -1.08 V, due to Mo VI/MoV and MoV/MoIV processes. Catalytic potential of these complexes was tested for the oxidation of benzoin using 30% aqueous H2O2 as an oxidant in methanol. At least four reaction products, benzoic acid, benzaldehyde-dimethylacetal, methyl benzoate and benzil were obtained with the 95-99% conversion under optimized reaction conditions. Oxidative bromination of salicylaldehyde, a functional mimic of haloperoxidases, in aqueous H2O2/KBr in the presence of HClO4 at room temperature has also been carried out successfully.

Synthesis, structural characterization and thermal properties of three copper(II) complexes based on aryl hydrazide ligands

Liu, Ming-Li,Dou, Jian-Min,Li, Da-Cheng,Wang, Da-Qi,Cui, Jian-Zhong

experimental part, p. 117 - 124 (2012/09/25)

The thiosemicarbazide and hydrazide Cu(II) complexes, [Cu3L 21(py)4Cl2] (1), [Cu(HL 2)py] (2) and [Cu(HL3)py] (3), (H2L1 = 1-picolinoylthiosemicarbazide, H

Magnesium(II), Zinc(II), Cadmium(II), Mercury(II) and Lead(II) Complexes of Salicylidene-Aroyl Hydrazides

Dutta, R. L.,Hossain, Md. Munkir

, p. 985 - 988 (2007/10/02)

Magnesium(II), zinc(II), cadmium(II), mercury(II) and lead(II) complexes of (substituted) salicylidene-benzoyl hydrazide, salicylidene-2-picoloyl hydrazide, salicylidene-2-quinoloyl hydrazide and salicylidene-8-quinoloyl hydrazide schiff bases have been s

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