329-84-0

Usage

Uses

Used in Organic Synthesis:
N'-Cyclohexylidene-p-nitrobenzhydrazide is used as a building block in the synthesis of diverse functional organic compounds, leveraging its unique structure and reactivity to facilitate the creation of complex molecules.
Used in Pharmaceutical and Agrochemical Preparation:
N'-Cyclohexylidene-p-nitrobenzhydrazide is employed as a key intermediate in the preparation of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and agricultural products.
Used in Dyes and Pigments Production:
N'-Cyclohexylidene-p-nitrobenzhydrazide is utilized in the production of dyes and pigments, where its chemical properties are harnessed to create a variety of colorants for different applications.
Used in Medicinal Chemistry:
It has been studied for its potential applications in medicinal chemistry, indicating its role in the discovery and development of new therapeutic agents.
Used as a Reagent for Analyte Detection:
N'-Cyclohexylidene-p-nitrobenzhydrazide is used as a reagent for the detection of certain analytes, highlighting its versatility in analytical chemistry for identifying and quantifying specific substances.

Upstream product

• 108-94-1 cyclohexanone 
• 636-97-5 N-amino-(4-nitrophenyl)carboxamide 

Downstream Products

• 1260116-80-0 diethyl {1-[2-(4-nitrobenzoyl)hydrazino]cyclohexyl}phosphonate 
• 63313-11-1 Ni(C₅H₁₀CNNCOC₆H₄NO₂-p)2 

Relevant academic research and scientific papers

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

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

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

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

Benzoylhydrazones in catalytic hydrophosphorylation

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