108347-23-5 Usage
Description
2,5-Dicarboxylic acid-3,4-ethylenedioxythiophene, also known as EDOT-2,5-dicarboxylic acid, is a chemical compound that serves as a key intermediate in the synthesis of conducting polymers. It is derived from the conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT) and features two carboxylic acid functional groups at the 2 and 5 positions of the thiophene ring. These functional groups facilitate the attachment of EDOT-2,5-dicarboxylic acid to other molecules, making it a versatile building block for the development of functional materials in various applications.
Uses
Used in Organic Electronic Devices:
2,5-Dicarboxylic acid-3,4-ethylenedioxythiophene is used as a key component in the synthesis of conducting polymers for organic electronic devices. The carboxylic acid groups enhance the solubility and processability of the resulting polymers, enabling their use in applications such as organic solar cells, organic light-emitting diodes (OLEDs), and organic field-effect transistors (OFETs).
Used in Sensors:
In the sensor industry, 2,5-Dicarboxylic acid-3,4-ethylenedioxythiophene is utilized as a building block for the development of conducting polymers with high sensitivity and selectivity towards various analytes. The carboxylic acid groups allow for the functionalization of the polymers, enabling the creation of sensors with tailored properties for detecting gases, ions, or biomolecules.
Used in Drug Delivery Systems:
2,5-Dicarboxylic acid-3,4-ethylenedioxythiophene is employed as a component in the design of drug delivery systems, particularly for the development of polymeric carriers with enhanced biocompatibility and water solubility. The carboxylic acid groups facilitate the attachment of therapeutic agents to the polymer backbone, allowing for controlled release and targeted delivery of drugs.
Used in Biomedical Applications:
In the biomedical field, 2,5-Dicarboxylic acid-3,4-ethylenedioxythiophene is used as a building block for the synthesis of biocompatible polymers with potential applications in tissue engineering, regenerative medicine, and implantable devices. The carboxylic acid groups contribute to the improved water solubility and biocompatibility of the resulting polymers, making them suitable for use in contact with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 108347-23-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,4 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 108347-23:
(8*1)+(7*0)+(6*8)+(5*3)+(4*4)+(3*7)+(2*2)+(1*3)=115
115 % 10 = 5
So 108347-23-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O6S/c9-7(10)5-3-4(14-2-1-13-3)6(15-5)8(11)12/h1-2H2,(H,9,10)(H,11,12)
