6319-28-4

Basic information

• Product Name: (E)-bis(2,5-dimethoxyphenyl)diazene
• CAS NO: 6319-28-4
• Molecular Formula: C₁₆H₁₈N₂O₄
• Molecular Weight: 302.3251
• Mol File: 6319-28-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 462.1°C at 760 mmHg
• Flash Point: 187.3°C
• Density: 1.14g/cm³
• Vapor Pressure: 2.79E-08mmHg at 25°C
• Refractive Index: 1.531
• CAS DataBase Reference: (E)-bis(2,5-dimethoxyphenyl)diazene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-bis(2,5-dimethoxyphenyl)diazene(6319-28-4)
• EPA Substance Registry System: (E)-bis(2,5-dimethoxyphenyl)diazene(6319-28-4)

Safety Data

• Hazardous Substances Data: 6319-28-4(Hazardous Substances Data)

Usage

General Description

(E)-bis(2,5-dimethoxyphenyl)diazene is a chemical compound with the molecular formula C18H22N2O2. It is a diazene compound, which is a class of organic compounds containing the functional group with the formula RN=NR. This specific compound has two 2,5-dimethoxyphenyl groups attached to the diazene functional group in a trans configuration. Its exact properties and uses are not widely documented, but diazene compounds have been studied for their potential applications in the field of organic chemistry, particularly as reactive intermediates in various synthetic reactions. Additionally, diazene compounds have been investigated for their biological activities and potential pharmaceutical applications. Further research is needed to fully understand the properties and potential uses of (E)-bis(2,5-dimethoxyphenyl)diazene.

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Relevant articles and documents

Quantification and evaluation of kinetic bio-catalytic pathway of horseradish peroxidase in an electron mediated reaction system and its applications in plant extracts

The intermolecular coupling of 2,5-dimethoxyaniline (DMA) as mediated electron transfer reaction in presence of H2O2 and peroxidase in acetate buffer of pH 4.2 resulting green colored product having maximum absorption at λmax = 740 nm was investigated by spectrophotometer. Under optimum conditions, linearity range for the quantification of H2O2 was 2.0-288.0 μM and for peroxidase were 0.59-9.46 and 0.443-9.46 nM by kinetic and fixed-time method, respectively. The catalytic efficiency and catalytic power were KeffD = 2.354 × 105 M-1 min-1 and KpowD = 4.59 × 10-4 min-1, respectively. From the plot of d(1/D o) vs d(1/Vo) and d(1/Ho) vs d(1/V o), Michaelis-Menten constants for DMA and H2O 2were found that KmD = 1458 μM and KmH2O2 = 301 μM. Applicability of the method was tested for peroxidase activity in some plant extracts and compared with guaiacol/peroxidase system. Regarding superiority of the method, it is suggested that DMA/peroxidase system can be a better hydrogen donor for HRP assay than guaiacol system as evident from kinetic data.