60511-85-5 Usage
Uses
Used in Materials Science:
11,12-Dihydroindolo[2,3-a]carbazole is used as a building block for the development of novel materials due to its unique structure and properties, contributing to the advancement of materials with specific characteristics for various applications.
Used in Organic Electronics:
In the field of organic electronics, 11,12-Dihydroindolo[2,3-a]carbazole is used as a component in the design and synthesis of organic semiconductors, potentially enhancing the performance of electronic devices such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs).
Used in Pharmaceutical Industry:
11,12-Dihydroindolo[2,3-a]carbazole is used as a precursor in the synthesis of pharmaceutical compounds, leveraging its unique chemical properties to develop new drugs with potential therapeutic applications.
Used in Biological Research:
11,12-Dihydroindolo[2,3-a]carbazole is used as a cytotoxic agent in biological research, being studied for its potential effects on various types of cells, which could lead to the discovery of new treatments for diseases.
Each of these applications highlights the diverse utility of 11,12-Dihydroindolo[2,3-a]carbazole, underscoring its importance in the ongoing development of new technologies and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 60511-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,1 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60511-85:
(7*6)+(6*0)+(5*5)+(4*1)+(3*1)+(2*8)+(1*5)=95
95 % 10 = 5
So 60511-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H12N2/c1-3-7-15-11(5-1)13-9-10-14-12-6-2-4-8-16(12)20-18(14)17(13)19-15/h1-10,19-20H
60511-85-5Relevant articles and documents
An efficient and general synthesis of indolo[2,3-a]carbazoles using the Fischer indole synthesis
Hu, Yong-Zhou,Chen, You-Qin
, p. 42 - 48 (2007/10/03)
Synthetically important indolo[2,3-a]carbazoles were obtained in a one-pot reaction via Fischer indole synthesis starting from 2-amino-cyclohexanone hydrochloride and substituted arylhydrazines hydrochloride in the presence of acidic media.
