20057-16-3

Basic information

• Product Name: 5,10-dihydro-5-methylphenazine
• Synonyms: 5,10-dihydro-5-methylphenazine;Phenazine, 5,10-dihydro-5-methyl-
• CAS NO: 20057-16-3
• Molecular Formula: C₁₃H₁₂N₂
• Molecular Weight: 196.2478
• Mol File: 20057-16-3.mol
• Article Data: 9

Chemical Properties

• Melting Point: 164-165 °C
• Boiling Point: 346.5°Cat760mmHg
• Flash Point: 169.6°C
• Appearance: /
• Density: 1.133g/cm³
• Vapor Pressure: 5.72E-05mmHg at 25°C
• Refractive Index: 1.619
• PKA: 6.25±0.20(Predicted)
• CAS DataBase Reference: 5,10-dihydro-5-methylphenazine(CAS DataBase Reference)
• NIST Chemistry Reference: 5,10-dihydro-5-methylphenazine(20057-16-3)
• EPA Substance Registry System: 5,10-dihydro-5-methylphenazine(20057-16-3)

Safety Data

• Hazardous Substances Data: 20057-16-3(Hazardous Substances Data)

Usage

Description

5,10-dihydro-5-methylphenazine is an organic compound characterized by its unique molecular structure, which features a phenazine core with a methyl group at the 5-position and hydrogen atoms at the 5 and 10 positions. 5,10-dihydro-5-methylphenazine is known for its ability to participate in electron-transfer reactions, making it a valuable component in various analytical and industrial applications.

Uses

Used in Analytical Chemistry:
5,10-dihydro-5-methylphenazine is used as a redox-active compound for electron-transfer reaction analyses. Its ability to participate in electron transfer makes it a useful tool in studying redox processes, which are essential in various chemical and biological systems.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5,10-dihydro-5-methylphenazine is used as a starting material or intermediate in the synthesis of various drugs and drug candidates. Its unique redox properties can be exploited to develop novel therapeutic agents with potential applications in treating different diseases.
Used in Environmental Monitoring:
5,10-dihydro-5-methylphenazine can be employed as a sensor or indicator in environmental monitoring, particularly for detecting and quantifying redox-active pollutants or contaminants. Its sensitivity to electron-transfer reactions allows for the development of reliable and accurate monitoring systems.
Used in Material Science:
In the field of material science, 5,10-dihydro-5-methylphenazine can be utilized in the development of novel materials with specific electronic properties. Its redox activity can be integrated into the design of advanced materials for applications such as energy storage, sensors, and electronic devices.
Used in Chemical Synthesis:
5,10-dihydro-5-methylphenazine serves as a versatile building block in chemical synthesis, particularly for the preparation of complex organic molecules and pharmaceutical compounds. Its unique structure and redox properties make it a valuable component in the synthesis of various target molecules with potential applications in various industries.

InChI:InChI=1/C13H12N2/c1-15-12-8-4-2-6-10(12)14-11-7-3-5-9-13(11)15/h2-9,14H,1H3

Upstream product

• 613-32-1 5,10-dihydrophenazine 
• 74-88-4 methyl iodide 
• 7432-06-6 5-methylphenazinium 
• 46406-08-0 10-methyl-5(10H)-phenazinyl 
• 92-82-0 Phenazin 
• 77-78-1 dimethyl sulfate 
• 58971-05-4 1,4-dihydropyridine-1-phenyl-3-carboxamide 
• 67146-57-0 1,1'-dibenzyl-1,4,1',4'-tetrahydro-[4,4']bipyridinyl-3,3'-dicarboxylic acid diamide 
• 1451492-40-2 C₂₈H₃₀N₄O₂ 
• 1451492-37-7 C₂₈H₃₀N₄O₄ 
• 7432-06-6 5-Methyl-phenaziniumkation-Radikal 
• 299-11-6 phenazine methosulfate 

Downstream Products

• 125106-21-0 5-(3,5-Dinitro-benzyl)-10-methyl-5,10-dihydro-phenazine; compound with 2-(4-dicyanomethylene-cyclohexa-2,5-dienylidene)-malononitrile 
• 125106-19-6 5-Methyl-10-(4-nitro-benzyl)-5,10-dihydro-phenazine; compound with 2-(4-dicyanomethylene-cyclohexa-2,5-dienylidene)-malononitrile 
• 125106-20-9 5-Methyl-10-(3-nitro-benzyl)-5,10-dihydro-phenazine; compound with 2-(4-dicyanomethylene-cyclohexa-2,5-dienylidene)-malononitrile 
• 125106-22-1 4-(10-Methyl-10H-phenazin-5-ylmethyl)-benzonitrile; compound with 2-(4-dicyanomethylene-cyclohexa-2,5-dienylidene)-malononitrile 
• 125108-13-6 3-(10-Methyl-10H-phenazin-5-ylmethyl)-benzonitrile; compound with 2-(4-dicyanomethylene-cyclohexa-2,5-dienylidene)-malononitrile 
• 125106-18-5 5-Benzyl-10-methyl-5,10-dihydro-phenazine; compound with 2-(4-dicyanomethylene-cyclohexa-2,5-dienylidene)-malononitrile 
• 299-11-6 phenazine methosulfate 
• 3331-28-0 2-bromophenazine 
• 100-13-0 4-nitrostyrene 
• 125106-07-2 5-methyl-10-(3,5-dinitrobenzyl)-5,10-dihydrophenazine 
• 125106-04-9 5-methyl-10-benzyl-5,10-dihydrophenazine 
• 63508-56-5 10-methyl-2(10H)-phenathiazineone 
• 92-82-0 Phenazin 

Relevant articles and documents

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A classical but new kinetic equation for hydride transfer reactions

A classical but new kinetic equation to estimate activation energies of various hydride transfer reactions was developed according to transition state theory using the Morse-type free energy curves of hydride donors to release a hydride anion and hydride acceptors to capture a hydride anion and by which the activation energies of 187 typical hydride self-exchange reactions and more than thirty thousand hydride cross transfer reactions in acetonitrile were safely estimated in this work. Since the development of the kinetic equation is only on the basis of the related chemical bond changes of the hydride transfer reactants, the kinetic equation should be also suitable for proton transfer reactions, hydrogen atom transfer reactions and all the other chemical reactions involved with breaking and formation of chemical bonds. One of the most important contributions of this work is to have achieved the perfect unity of the kinetic equation and thermodynamic equation for hydride transfer reactions. The Royal Society of Chemistry.

Thermally Unstable 5-(9-Anthrylmethyl)-10-methyl-5,10-dihydrophenazine

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