531-47-5

Basic information

• Product Name: 5,12-DIHYDRO-5,7,12,14-TETRAZAPENTACENE
• Synonyms: 5,12-DIHYDRO-5,7,12,14-TETRAZAPENTACENE;5,12-Dihydroquinoxalino[2,3-b]phenazine;7,14-Dihydroquinoxalino[2,3-b]phenazine;Homofluorindine;5,12-Dihydro-5,7,12,14-tetraazapentacene
• CAS NO: 531-47-5
• Molecular Formula: C₁₈H₁₂N₄
• Molecular Weight: 284.31
• Product Categories: Aromatics;Fluorescent Labels & Indicators;Heterocycles
• Mol File: 531-47-5.mol

Chemical Properties

• Melting Point: 545 °C
• Boiling Point: 431.5±45.0 °C(Predicted)
• Appearance: /
• Density: 1.43
• PKA: 8.38±0.20(Predicted)
• CAS DataBase Reference: 5,12-DIHYDRO-5,7,12,14-TETRAZAPENTACENE(CAS DataBase Reference)
• NIST Chemistry Reference: 5,12-DIHYDRO-5,7,12,14-TETRAZAPENTACENE(531-47-5)
• EPA Substance Registry System: 5,12-DIHYDRO-5,7,12,14-TETRAZAPENTACENE(531-47-5)

Safety Data

• Hazardous Substances Data: 531-47-5(Hazardous Substances Data)

Usage

Uses

Used in Immunochemical Applications:
5,12-Dihydro-5,7,12,14-Tetrazapentacene is used as a substrate with chemiluminescence amplification for immunochemical use. Its chemiluminescent properties allow for enhanced detection and analysis of target molecules in immunoassays, providing increased sensitivity and accuracy in the identification and quantification of specific antigens or antibodies.
Used in Diagnostic Industry:
In the diagnostic industry, 5,12-Dihydro-5,7,12,14-Tetrazapentacene is used as a chemiluminescent substrate to improve the detection of various biomarkers and disease indicators. Its ability to amplify chemiluminescence signals enables more accurate and sensitive diagnostic tests, contributing to better patient care and disease management.
Used in Research and Development:
5,12-Dihydro-5,7,12,14-Tetrazapentacene is also utilized in research and development for the creation of new immunoassay techniques and the study of molecular interactions. Its unique chemiluminescent properties make it a valuable tool for scientists to explore novel methods in immunochemistry and enhance the understanding of biological processes.

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Relevant articles and documents

A benzoquinone-derived porous hydrophenazine framework for efficient and reversible iodine capture

A type of benzoquinone-derived porous organic polymer with hydrophenazine linkages, porous hydrophenazine frameworks, has been developed. Their application in iodine capture from both air and solution was investigated.

A mild and simple method for the synthesis of substituted phenazines

A mild, simple, and general method has been developed for the synthesis of phenazines by cross-coupling of benzoquinones with o-phenylenediamines. Benzoquinones and o-phenylenediamines reacted smoothly to give the corresponding cross-coupled products in good to excellent yields. 1,4-Naphthoquinone also coupled with o-phenylenediamines in the presence of copper acetate at 50? °C to give the corresponding benzo[a]phenazines. All reactions could be carried out under air. Georg Thieme Verlag Stuttgart New York.

Organic thin film transistors based on stable amorphous ladder tetraazapentacenes semiconductors

Three ladder linear 5,7,12,14-tetraazapentacenes (1-3) have been synthesized by an improved condensation reaction with high yields. These tetraazapentacenes show higher thermal and optical stability in solution and solid films compared to pentacene. Organic thin film transistors (OTFTs) based on amorphous films of 5,7,12,14-tetraazapentacene are investigated in this contribution. A field-effect mobility of a stable amorphous OTFT in air up to 2 × 10-2 cm2 V-1 s-1 has been achieved. The high stability and high mobility in the amorphous state of ladder compounds 1-3 combined with the easy synthesis make them a new family of promising candidate for organic electronic devices. The Royal Society of Chemistry 2005.