2074-04-6

Basic information

• Product Name: (2E)-1-(2,4-dinitrophenyl)-2-(2-phenylethylidene)hydrazine
• CAS NO: 2074-04-6
• Molecular Formula: C₁₄H₁₂N₄O₄
• Molecular Weight: 300.2695
• Mol File: 2074-04-6.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 488.1°C at 760 mmHg
• Flash Point: 249°C
• Density: 1.35g/cm³
• Vapor Pressure: 1.12E-09mmHg at 25°C
• Refractive Index: 1.637
• CAS DataBase Reference: (2E)-1-(2,4-dinitrophenyl)-2-(2-phenylethylidene)hydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-1-(2,4-dinitrophenyl)-2-(2-phenylethylidene)hydrazine(2074-04-6)
• EPA Substance Registry System: (2E)-1-(2,4-dinitrophenyl)-2-(2-phenylethylidene)hydrazine(2074-04-6)

Safety Data

• Hazardous Substances Data: 2074-04-6(Hazardous Substances Data)

Usage

Description

(2E)-1-(2,4-dinitrophenyl)-2-(2-phenylethylidene)hydrazine is a hydrazine derivative with the chemical formula C16H14N6O4. It features a dinitrophenyl group and a phenylethylidene group, which contribute to its unique chemical properties.

Uses

Used in Chemical Research:
(2E)-1-(2,4-dinitrophenyl)-2-(2-phenylethylidene)hydrazine is utilized as a research compound for studying its chemical behavior and potential applications in various chemical processes. Its strong electron-withdrawing dinitrophenyl group and the presence of a phenylethylidene group make it an interesting subject for scientific investigation.
Due to the limited information provided and the compound's relative obscurity, the specific uses and applications of (2E)-1-(2,4-dinitrophenyl)-2-(2-phenylethylidene)hydrazine are not widely known. Further research may reveal additional uses in different industries or for specific purposes.

Upstream product

• 100-42-5 styrene 
• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 
• 122-78-1 phenylacetaldehyde 
• 4861-85-2 isopropyl phenylacetate 
• 101-41-7 benzeneacetic acid methyl ester 
• 101-97-3 Ethyl 2-phenylethanoate 
• 60-12-8 2-phenylethanol 
• 102-16-9 benzyl 2-phenylacetate 
• 97-00-7 1-chloro-2,4-dinitro-benzene 
• 100-34-5 benzene diazonium chloride 
• 39153-68-9 (E,Z)-β-phenoxystyrene 
• 182222-85-1 1-chloro-1-butoxy-2-phenylethane 
• 36586-17-1 (E)-(2-butoxyethenyl)benzene 
• 124337-51-5 9-(1-Benzotriazol-1-yl-2-phenyl-ethyl)-9H-carbazole 

Downstream Products

• 4881-02-1 2-Phenyl-2-propoxy-acetaldehyd-<2.4-dinitro-phenylhydrazon> 
• 4881-00-9 2-Methoxy-2-phenyl-acetaldehyd-<2.4-dinitro-phenylhydrazon> 
• 4881-05-4 2-tert-Butoxy-2-phenyl-acetaldehyd-<2.4-dinitro-phenylhydrazon> 
• 4881-01-0 2-Aethoxy-2-phenyl-acetaldehyd-<2.4-dinitro-phenylhydrazon> 

Relevant articles and documents

Proton abstraction and electrophilic quench at C-2 of imidazolidines

Imidazolidines bearing tert-butoxycarbonyl groups on both nitrogen atoms have been prepared in order to test their ability to act as acyl anion equivalents. Proton abstraction was achieved successfully at C-2, between the two nitrogen atoms, using the bas

Selective Hydrosilylation of Esters to Aldehydes Catalysed by Iridium(III) Metallacycles through Trapping of Transient Silyl Cations

The combination of an iridium(III) metallacycle and 1,3,5-trimethoxybenzene catalyses rapidly and selectively the reduction of esters to aldehydes at room temperature with high yields through hydrosilylation followed by hydrolysis. The ester reduction involves the trapping of transient silyl cations by the 1,3,5-trimethoxybenzene co-catalyst, supposedly by formation of an arenium intermediate whose role was addressed by DFT calculations.

2-Iodoxybenzoic acid organosulfonates: Preparation, X-ray structure and reactivity of new, powerful hypervalent iodine(v) oxidants

New powerful hypervalent iodine(v) oxidants, tosylate and mesylate derivatives of 2-iodoxybenzoic acid (IBX), were prepared by the reaction of IBX with the corresponding sulfonic acids. Single crystal X-ray crystallography of the diacetate derivative of IBX-tosylate revealed an unusual heptacoordinated iodine geometry without any significant intermolecular secondary interactions.