2829-25-6

Basic information

• Product Name: 1-(4-methylbenzylidene)-2-phenylhydrazine
• CAS NO: 2829-25-6
• Molecular Formula: C₁₄H₁₄N₂
• Molecular Weight: 210.2744
• Mol File: 2829-25-6.mol
• Article Data: 38

Chemical Properties

• Boiling Point: 340.6°C at 760 mmHg
• Flash Point: 159.8°C
• Density: 1g/cm³
• Vapor Pressure: 8.51E-05mmHg at 25°C
• Refractive Index: 1.561
• CAS DataBase Reference: 1-(4-methylbenzylidene)-2-phenylhydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methylbenzylidene)-2-phenylhydrazine(2829-25-6)
• EPA Substance Registry System: 1-(4-methylbenzylidene)-2-phenylhydrazine(2829-25-6)

Safety Data

• Hazardous Substances Data: 2829-25-6(Hazardous Substances Data)

Usage

General Description

1-(4-methylbenzylidene)-2-phenylhydrazine is a chemical compound with the molecular formula C15H14N2. It is a hydrazine derivative with a benzylidene group and a phenyl group attached to the hydrazine nitrogen atoms. 1-(4-methylbenzylidene)-2-phenylhydrazine is commonly used in organic synthesis and chemical research as a reagent or intermediate. It has potential applications in the pharmaceutical industry, particularly in the development of antitumor agents and other medicinal compounds. Additionally, 1-(4-methylbenzylidene)-2-phenylhydrazine has been studied for its antimicrobial and antifungal properties, making it a valuable chemical for various scientific and industrial purposes.

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 100-63-0 phenylhydrazine 
• 827-71-4 4-methyl-benzimidic acid ethyl ester 
• 589-18-4 4-Methylbenzyl alcohol 
• 59-88-1 phenylhydrazine hydrochloride 
• 62-53-3 aniline 
• 25939-01-9 p-toluoyl chloride phenylhydrazone 
• 7559-36-6 4-methyl-β-nitrostyrene 
• 586-96-9 Nitrosobenzene 
• 104-84-7 para-methylbenzylamine 

Downstream Products

• 101773-50-6 (E)-1-(2'-p-methylbenzylidene-1'-phenylhydrazinyl)1,2-dibenzoylethylene 
• 1622-12-4 1,5-Diphenyl-3-p-methylphenylformazan 
• 104-87-0 4-methyl-benzaldehyde 
• 104707-44-0 C₁₅H₁₃ClN₂O 
• 7684-30-2 N,N-dimethyl-N'-phenylcarbamimidic chloride 
• 104-85-8 para-methylbenzonitrile 
• 1132-39-4 diphenylselenide 
• 99-94-5 p-Toluic acid 
• 1622-12-4 3-(p-methylphenyl)-1,5-diphenylformazan 
• 80165-57-7 2-(4-methylbenzylidene)-1-benzyl-1-phenylhydrazine 
• 23982-82-3 1-benzyl-2-(4-methylphenyl)-1H-benzimidazole 
• 158470-48-5 3-(4-methylphenyl)-1-phenyl-4H-indeno[2,3-d]pyrazole 
• 1220278-14-7 diethyl 3-(p-methylphenyl)-(1H)-1-phenylpyrazole-4,5-dicarboxylate 
• 1220278-11-4 dimethyl (1H)-1-phenyl-3-(p-methylphenyl)pyrazole-4,5-dicarboxylate 

Relevant articles and documents

Formazanate ligands as structurally versatile, redox-active analogues of β-diketiminates in zinc chemistry

A range of tetrahedral bis(formazanate)zinc complexes with different steric and electronic properties of the formazanate ligands were synthesized. The solid-state structures for several of these were determined by X-ray crystallography, which showed that

Sequential [3+2] annulation reaction of prop-2-ynylsulfonium salts and hydrazonyl chlorides: Synthesis of pyrazoles containing functional motifs

A novel sequential [3+2] annulation reaction has been developed using prop-2-ynylsulfonium salts and hydrazonyl chlorides, affording a series of pyrazoles with functional motifs that can be post modified in the preparation of various drugs or drug candidates. Further transformation and gram-scale operations could also be achieved efficiently. This journal is

Synthesis of 1,1′-([1,1′-Biphenyl]-4,4′-diyl)bis(3-aryl-5-phenylformazans) and 1,1′-([1,1′-Biphenyl]-4,4′-diyl)bis(3-aryl-5-phenyl-5,6-dihydro-1,2,4,5-tetrazin-1-ium) Perchlorates

Abstract: New bis-formazans and bis(5,6-dihydro-1,2,4,5-tetrazin-1-ium) perchlorates were synthesized with high yields under mild conditions. 1,1′-([1,1′-Biphenyl]-4,4′-diyl)bis(3-aryl-5-phenylformazans) were obtained by diazo coupling of para-substituted benzaldehyde phenylhydrazones with [1,1′-biphenyl]-4,4′-bis(diazonium chloride). Treatment of the obtained bis-formazans with formaldehyde in the presence of perchloric acid in dioxane afforded 1,1′-([1,1′-biphenyl]-4,4′-diyl)bis(3-aryl-5-phenyl-5,6-dihydro-1,2,4,5-tetrazin-1-ium) diper-chlorates. The structure of the synthesized compounds was confirmed by elemental analyses and UV, IR, and 1H and 13C NMR spectra.