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4-methyl-N-[(2-oxonaphthalen-1-ylidene)methyl]benzohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82859-80-1

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82859-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82859-80-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,5 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82859-80:
(7*8)+(6*2)+(5*8)+(4*5)+(3*9)+(2*8)+(1*0)=171
171 % 10 = 1
So 82859-80-1 is a valid CAS Registry Number.

82859-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-N-(p-tolyl)piperazine-1-carboxamide

1.2 Other means of identification

Product number -
Other names 4-methyl-N'-[(2-hydroxy-1-naphthyl)methylidene]benzohydrazide

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:82859-80-1 SDS

82859-80-1Downstream Products

82859-80-1Relevant articles and documents

Structure and biological properties of five Pt(II) complexes as potential anticancer agents

Deng, Jungang,Wang, Jun,Khan, MuhammadHamid,Yu, Ping,Yang, Feng,Liang, Hong

, p. 10 - 16 (2018/05/23)

We synthesized and validated five Schiff base Pt(II) complexes derived from 2-hydroxy-1-naphthaldehyde benzoyl hydrazone and its derivatives, which are modified at the benzohydrazide structures (L1–L5). The complexes were [Pt(L1)(DMSO)Cl] (C1), [Pt(L2)(DM

Arylation of N-Methyl-2-oxindole with Arylboronic Acids in Water Catalyzed by Palladium(II) Pincer Complexes with a Low Catalyst Loading

Vignesh, Arumugam,Kaminsky, Werner,Dharmaraj, Nallasamy

, p. 910 - 914 (2017/03/27)

Two new PdII ONO pincer complexes were utilized efficiently as homogeneous catalysts for the site-selective C3-arylation of N-methyl-2-oxindole with arylboronic acids at room temperature in aqueous media to yield a series of 3-aryl-N-methyl-2-oxindoles. This catalytic reaction progressed well with a low catalyst loading (0.01 mol %) under open-flask conditions. Notably, a column-chromatography-free method for the quantitative preparation of C3-arylated N-methyl-2-oxindoles is reported. The catalyst showed good compatibility with wide range of substrates with recyclability in up to five consecutive runs without an appreciable loss of yield.

Synthesis, characterization, structures, and catalytic property of oxovanadium(V) complexes with hydrazone ligands

Wang,Guo,Hu

, p. 891 - 895 (2014/02/14)

The reaction of [VO(Acac)2] with 4-methyl-N'-[(2-hydroxy-1- naphthyl)methylidene]benzohy- drazide (H2L1) and 4-methyl-N'-[1-(2-hydroxynaphthyl)ethyiidene]benzohydrazide (H2L 2), respectively, in metha

Synthesis of New Acylhydrazones as Iron-Chelating Compounds

Edward, John T.,Gauthier, Mario,Chubb, Francis L.,Ponka, Premysl

, p. 538 - 540 (2007/10/02)

Fourteen acylhydrazides have been condensed with three aromatic o-hydroxy aldehydes (pyridoxal, salicylaldehyde, and 2-hydroxy-1-naphthaldehyde) to give 42 acylhydrazones, of which 38 are new.These compounds complex iron and have shown varying abilities to promote the movement of iron across biological membranes.Their infrared and nuclear magnetic resonance spectra support the structures assigned to them.

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