23062-43-3 Usage
Uses
Used in Organic Synthesis:
Indenothiophenone is utilized as a key intermediate in the synthesis of various organic compounds, contributing to the development of new chemical entities with diverse applications.
Used in Organic Electronics:
In the field of organic electronics, indenothiophenone is employed as a component in the design and fabrication of electronic devices, leveraging its electronic properties to enhance device performance.
Used in Material Science:
Indenothiophenone is used as a building block in the creation of novel materials with specific properties, such as conductivity or stability, for applications in various industries.
Used in Drug Discovery and Development:
Indenothiophenone is studied for its potential pharmacological activities, making it a candidate for the development of new drugs, particularly in the context of its biological effects and interactions.
Used in Pharmaceutical Industry:
8H-Indeno[1,2-c]thiophen-8-one is used as a chemical entity in the pharmaceutical industry for its potential therapeutic applications, based on its pharmacological properties and the ongoing research into its medicinal uses.
Check Digit Verification of cas no
The CAS Registry Mumber 23062-43-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,6 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23062-43:
(7*2)+(6*3)+(5*0)+(4*6)+(3*2)+(2*4)+(1*3)=73
73 % 10 = 3
So 23062-43-3 is a valid CAS Registry Number.
23062-43-3Relevant academic research and scientific papers
Photochemical generation of thiophene analogs of 9-fluorenyl cations
Bancerz, Mathew,Huck, Lawrence A.,Leigh, William J.,Mladenova, Gabriela,Najafian, Katayoun,Zeng, Xiaofeng,Lee-Ruff, Edward
, p. 1202 - 1213 (2011/09/12)
The 9-fluorenyl cation is a member of the 4N Hueckel antiaromatic series of intermediates, first observed by time-resolved spectroscopy on UV photo-excitation of 9-fluorenol. Thiophene analogs of 9-fluorenol in which one of the annelated benzene rings is
