75912-31-1

Basic information

• Product Name: 1-(4-nitrophenyl)-2-(pentan-3-ylidene)hydrazine
• CAS NO: 75912-31-1
• Molecular Formula: C₁₁H₁₅N₃O₂
• Molecular Weight: 221.2557
• Mol File: 75912-31-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 344.3°C at 760 mmHg
• Flash Point: 162°C
• Density: 1.13g/cm³
• Vapor Pressure: 6.66E-05mmHg at 25°C
• Refractive Index: 1.552
• CAS DataBase Reference: 1-(4-nitrophenyl)-2-(pentan-3-ylidene)hydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-nitrophenyl)-2-(pentan-3-ylidene)hydrazine(75912-31-1)
• EPA Substance Registry System: 1-(4-nitrophenyl)-2-(pentan-3-ylidene)hydrazine(75912-31-1)

Safety Data

• Hazardous Substances Data: 75912-31-1(Hazardous Substances Data)

Usage

General Description

1-(4-nitrophenyl)-2-(pentan-3-ylidene)hydrazine is a chemical compound with the molecular formula C15H18N4O2. It is a hydrazine derivative that contains a nitrophenyl group and a pentan-3-ylidene group. 1-(4-nitrophenyl)-2-(pentan-3-ylidene)hydrazine has potential applications in the field of chemistry and pharmaceutical science, and its properties and reactivity make it a valuable intermediate for the synthesis of other organic compounds. It is important to handle this compound with care, as it may pose health and environmental hazards if not properly managed. Additional research is needed to further explore its potential uses and properties.

Upstream product

• 100-16-3 4-nitrophenylhydrazone 
• 96-22-0 pentan-3-one 

Downstream Products

• 96-22-0 pentan-3-one 

Relevant articles and documents

Synthesis, spectral and structural studies, and an evaluation of the hydrogen bonding of some phenylhydrazones

A series of 46 phenylhydrazones, some novel, containing a variety of structural types has been synthesised. These have been studied by 1H n.m.r. and i.r. spectroscopy with respect to potential inter- and intra-molecular hydrogen bonding. ortho-Nitro or -carbonyl groups form strong hydrogen bonds to the imino-group which are readily observed by 1H n.m.r. but not by i.r. spectroscopy. 'Terminal' carbonyl groups also form strong hydrogen bonds to the imino-group and these can be detected by both i.r. and 1H n.m.r. spectroscopy. When both ortho-nitro- or -carbonyl groups and 'terminal' carbonyl groups are present the imino hydrogen atom is doubly hydrogen bonded and this is apparent in the 1H n.m.r. spectrum. The formation of an intramolecular hydrogen bond in the phenylhydrazone prevents the formation of an intermolecular hydrogen bond between the phenylhydrazone and a polar solvent.