329-84-0

Basic information

• Product Name: N'-Cyclohexylidene-p-nitrobenzhydrazide
• Synonyms: N'-Cyclohexylidene-p-nitrobenzhydrazide
• CAS NO: 329-84-0
• Molecular Formula: C₁₃H₁₅N₃O₃
• Molecular Weight: 0
• Mol File: 329-84-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N'-Cyclohexylidene-p-nitrobenzhydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: N'-Cyclohexylidene-p-nitrobenzhydrazide(329-84-0)
• EPA Substance Registry System: N'-Cyclohexylidene-p-nitrobenzhydrazide(329-84-0)

Safety Data

• Hazardous Substances Data: 329-84-0(Hazardous Substances Data)

Usage

General Description

N'-Cyclohexylidene-p-nitrobenzhydrazide is a chemical compound used in organic synthesis and as a reagent in chemical reactions. It is a yellow crystalline solid with the molecular formula C14H14N4O3. N'-Cyclohexylidene-p-nitrobenzhydrazide is commonly used in the preparation of various pharmaceuticals and agrochemicals, as well as in the production of dyes and pigments. Its unique structure and reactivity make it a valuable building block for the synthesis of diverse functional organic compounds. Additionally, it has been studied for its potential applications in medicinal chemistry and as a reagent for the detection of certain analytes.

Upstream product

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

Downstream Products

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

Relevant articles and documents

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

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