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6364-19-8

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6364-19-8 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.

Check Digit Verification of cas no

The CAS Registry Mumber 6364-19-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6364-19:
(6*6)+(5*3)+(4*6)+(3*4)+(2*1)+(1*9)=98
98 % 10 = 8
So 6364-19-8 is a valid CAS Registry Number.
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)

6364-19-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name perylene-3,9-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names Perylen-3,9-dicarbonsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6364-19-8 SDS

6364-19-8Relevant articles and documents

A 3, 9 - perylene dicarboxylic acid preparation method

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, (2019/03/23)

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 acid medicinal molecule with antineoplastic activity

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, (2019/01/08)

The invention discloses a preparation method and application of a novel perylene acid medicinal molecule with antineoplastic activity, and belongs to the technical field of pharmaceutical synthesis. The novel perylene acid medicinal molecule with antineoplastic activity is characterized by having the structural formula as shown in the description. The invention also provides a preparation method of the novel perylene medicinal molecule with the antineoplastic activity. The prepared perylene medicinal molecule has higher inhibiting activity for human cervical carcinoma Hela cells, human breastcancer MDA-MB-231 cells and human liver cancer HepG2 cells, and has the potential of becoming an antineoplastic medicament.

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