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N2-Cyclohexylidenebenzhydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24214-79-7

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24214-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24214-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,1 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24214-79:
(7*2)+(6*4)+(5*2)+(4*1)+(3*4)+(2*7)+(1*9)=87
87 % 10 = 7
So 24214-79-7 is a valid CAS Registry Number.

24214-79-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(cyclohexylideneamino)benzamide

1.2 Other means of identification

Product number -
Other names 1-benzoyl-2-cyclohexylidene-hydrazine

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:24214-79-7 SDS

24214-79-7Relevant academic research and scientific papers

Lanthanide-EDTA complexes covalently bonded on Fe3O4@SiO2 magnetic nanoparticles promote the green, stereoselective synthesis of: N-Acylhydrazones

De Resende Filho, Jo?o Batista M.,Falc?o, Nathália Kellyne S. M.,Pires, Gilvan P.,De Vasconcelos, Luiz Fernando S.,Pinheiro, Sávio M.,Dos Santos Filho, José Maurício,Fraz?o Barbosa, Marília Imaculada,Doriguetto, Ant?nio Carlos,Teotonio, Ercules E. S.,Vale, Juliana A.

, p. 14257 - 14269 (2019/09/30)

In the last few years, many synthetic methods have been developed using magnetic nanomaterial-based catalysts with considerable advantages for the efficiency, selectivity and applicability of green procedures. In this work, lanthanide-EDTA complexes coval

Stereoselective, solvent free, highly efficient synthesis of aldo- and keto-: N -acylhydrazones applying grindstone chemistry

Dos Santos Filho, José Maurício,Pinheiro, Savio Moita

supporting information, p. 2212 - 2224 (2017/07/24)

A mild and efficient synthesis of N-acylhydrazones has been developed, applying a simple grindstone procedure, leading to a library of 51 examples exhibiting a broad variety of structural features, 21 of them described for the first time in this paper. Th

Mild, Stereoselective, and Highly Efficient Synthesis of N-Acylhydrazones Mediated by CeCl3·7H2O in a Broad Range of Solvents

Dos Santos Filho, José Maurício

supporting information, p. 6411 - 6417 (2016/02/18)

In a mild and practical approach, hydrazides and aldehydes underwent condensation reactions that were mediated by cerium(III) chloride to be rapidly converted into N-acylhydrazones. This method uses a minimal catalytic amount of cerium(III), is stereosele

Fast synthesis of N-acylhydrazones employing a microwave assisted neat protocol

Andrade, Marta M.,Barros, Maria Teresa

supporting information; experimental part, p. 245 - 247 (2010/08/19)

A variety of N-acylhydrazones were synthesized under microwave irradiation within 2.5-10 min, starting from benzo, salicyloyl, and isonicotinic hydrazides. The protocol developed employs microwave irradiation in the absence of solvents and catalysts, lead

Benzoylhydrazones in catalytic hydrophosphorylation

Matveeva,Podrugina,Kolesnikova,Zefirov

experimental part, p. 411 - 417 (2011/02/17)

Reactions of benzoylhydrazones derived from heterocyclic and aromatic aldehydes and aliphatic, heterocyclic, and aliphatic-aromatic ketones with diethyl phosphite in the presence of [tetra(tert-butyl)phthalocyanine]aluminum chloride afford α-benzoylhydraz

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