6364-19-8

Basic information

• Product Name: 3,9-perylenedicarboxylic acid
• Synonyms: 3,9-perylenedicarboxylic acid;perylene-3,9-dicarboxylic acid;Einecs 228-852-0
• CAS NO: 6364-19-8
• Molecular Formula: C₂₂H₁₂O₄
• Molecular Weight: 340.32828
• EINECS: 228-852-0
• Mol File: 6364-19-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 694.3 °C at 760 mmHg
• Flash Point: 387.7 °C
• Appearance: /
• Density: 1.538 g/cm³
• Vapor Pressure: 3.07E-20mmHg at 25°C
• Refractive Index: 1.916
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 3.03±0.30(Predicted)
• CAS DataBase Reference: 3,9-perylenedicarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3,9-perylenedicarboxylic acid(6364-19-8)
• EPA Substance Registry System: 3,9-perylenedicarboxylic acid(6364-19-8)

Safety Data

• Hazardous Substances Data: 6364-19-8(Hazardous Substances Data)

Usage

General Description

3,9-perylenedicarboxylic acid is a polycyclic aromatic compound with the molecular formula C24H12O4. It is a derivative of perylene and is commonly used in the production of organic electronic materials, such as organic light emitting diodes (OLEDs) and organic photovoltaic cells (OPVs). 3,9-perylenedicarboxylic acid exhibits excellent thermal stability and high charge carrier mobility, making it a promising material for various electronic applications. Its strong π-π interactions also make it useful for the construction of self-assembled monolayers and multilayers on solid surfaces for applications in molecular electronics and sensors. Additionally, 3,9-perylenedicarboxylic acid has potential as a fluorescent dye for biomedical imaging and as a laser dye due to its strong and narrow emission spectrum in the visible region. Overall, this chemical has diverse applications in the field of materials science and electronics.

InChI:InChI=1/C22H12O4/c23-21(24)17-9-8-16-12-4-2-6-14-18(22(25)26)10-7-15(20(12)14)11-3-1-5-13(17)19(11)16/h1-10H,(H,23,24)(H,25,26)

Upstream product

• 83-32-9 acenaphthene 
• 128-69-8 perylene-3,4,9,10-tetracarboxylic acid 3,4:9,10-dianhydride 
• 103147-46-2 perylene-3,9-dicarbonitrile 
• 81-83-4 1,8-Naphthalimide 
• 81-84-5 1,8-Naphthalic anhydride 
• 208-96-8 acenaphthylene 
• 81-33-4 3,4,9,10-perylene tetracarboxyxlic acid diimide 

Downstream Products

• 198-55-0 PERYLENE 
• 47477-48-5 perylene-3,9-dicarbonyl chloride 
• 26556-97-8 3,9-dibenzoyl-perylene 
• 923584-56-9 perylene-3,10-dicarbonyl chloride 

Relevant articles and documents

A 3, 9 - perylene dicarboxylic acid preparation method

The invention discloses a 3, 9 - perylene dicarboxylic acid of preparation method, specific step is ice-acetic acid in a solvent, in the dihydro e is obtained under the action of the sodium dichromate of 1, 8 - naphthalenedicarboxylic anhydride; 1, 8 - naphthalenedicarboxylic anhydride in saturated ammonia under the action of the acylation to obtain the 1, 8 - naphthalene asia amide; 1, 8 - naphthalene asia amide in potassium hydroxide and anhydrous sodium acetate manufacturing of the alkaline environment in the alkaline environment in C - C under high-temperature conditions obtained by coupling the 3, 4, 9, 10 - perylenetetracarboxylic acid diimide; 3, 4, 9, 10 - perylenetetracarboxylic acid diimide in under the action of the strong acid is converted into the 3, 4, 9, 10 - [...]; 3, 4, 9, 10 - [...] in microwave reactor in alkaline hydrolysis by the decarboxylation of 3, 9 - perylene dicarboxylic acid. The invention synthetic process more economic, environmental protection, high-efficient and simple.

Preparation method and application of novel perylene drug molecule with biological activity

The invention discloses a preparation method and application of a novel perylene drug molecule with the biological activity, and belongs to the technical field of medicine synthesis. According to thekey points of the technical scheme of the preparation method and application of the novel perylene drug molecule, the structural formula of the perylene drug molecule with the biological activity is as shown in the specification, wherein R is O or S. The invention further relates to the preparation method for the novel perylene drug molecule with the biological activity. The perylene drug moleculeprepared through the preparation method has good inhibitory activity on human cervical cancer hHela cells, human breast cancer MDA-MB-231 cells and human liver cancer HepG2 cells, is relatively low in toxicity on human normal cells and has the potential of becoming an anti-tumor drug.