75343-45-2

Basic information

• Product Name: 1-[cyclopropyl(phenyl)methylidene]-2-(2,4-dinitrophenyl)hydrazine
• CAS NO: 75343-45-2
• Molecular Formula: C₁₆H₁₄N₄O₄
• Molecular Weight: 326.3068
• Mol File: 75343-45-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 490.6°C at 760 mmHg
• Flash Point: 250.5°C
• Density: 1.45g/cm³
• Vapor Pressure: 9E-10mmHg at 25°C
• Refractive Index: 1.691
• CAS DataBase Reference: 1-[cyclopropyl(phenyl)methylidene]-2-(2,4-dinitrophenyl)hydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[cyclopropyl(phenyl)methylidene]-2-(2,4-dinitrophenyl)hydrazine(75343-45-2)
• EPA Substance Registry System: 1-[cyclopropyl(phenyl)methylidene]-2-(2,4-dinitrophenyl)hydrazine(75343-45-2)

Safety Data

• Hazardous Substances Data: 75343-45-2(Hazardous Substances Data)

Usage

Type of compound

Hydrazine derivative

Structural features

Cyclopropyl(phenyl)methylidene group
2,4-Dinitrophenyl group attached to the hydrazine molecule

Usage

Organic synthesis
Reagent in chemical reactions

Potential applications

Pharmaceuticals
Agrochemicals

Versatility

Versatile reactivity
Ability to form a range of derivatives

Dinitrophenyl group

Useful marker in biochemical research and analysis

Upstream product

• 3481-02-5 cyclopropyl phenyl ketone 
• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 
• 74-85-1 ethene 
• 4023-34-1 cyclopropanecarboxylic acid chloride 
• 1007-03-0 1-phenyl-1-cyclopropylmethanol 

Downstream Products

• 3481-02-5 cyclopropyl phenyl ketone 
• 615-71-4 benzene-1,2,4-triamine 

Relevant articles and documents

Facile preparation and reactivity of bifunctional ionic liquid-supported hypervalent iodine reagent: A convenient recyclable reagent for catalytic oxidation

Novel, efficient, and recyclable bifunctional catalysts bearing ionic liquid supported (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) and iodoarene moieties were developed and used for environmentally benign catalytic oxidation of alcohols. The reactions using peracetic acid as a green and practical co-oxidant afforded the corresponding carbonyl compounds in high yields under mild conditions and convenient work-up. Furthermore, these ionic liquid supported bifunctional catalysts could be simply recovered and reused.