6558-83-4 Usage
General Description
1,8-DiMethylacarbazole is a chemical compound with the molecular formula C14H13N. It is a derivative of carbazole, an aromatic heterocyclic compound. 1,8-DiMethylacarbazole has been found to possess potential applications in organic electronics and optoelectronic devices, such as organic light-emitting diodes (OLEDs). Its unique structure and electronic properties make it a promising candidate for use in the development of new materials for these technologies. Additionally, 1,8-DiMethylacarbazole has also been studied for its potential use in the synthesis of organic semiconductors and as a component in the preparation of solar cells and other electronic devices. Overall, this chemical compound shows promise in various technological applications due to its unique properties and potential for use in the development of advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 6558-83-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6558-83:
(6*6)+(5*5)+(4*5)+(3*8)+(2*8)+(1*3)=124
124 % 10 = 4
So 6558-83-4 is a valid CAS Registry Number.
6558-83-4Relevant articles and documents
Reactions of arynes with nitrosoarenes - An approach to substituted carbazoles
Chakrabarty, Shyamal,Chatterjee, Indranil,Tebben, Ludger,Studer, Armido
, p. 2968 - 2971 (2013/03/29)
No transition metals are necessary in the reaction of in situ generated arynes with nitrosoarenes to give substituted carbazoles. Depending on the fluoride source and the solvent, either N-arylated carbazoles or NH-carbazoles are obtained (see scheme; DME=dimethoxyethane, OTf=trifluoromethanesulfonate). In these cascades a C-C and one or two C-N bonds are formed. The reactions are easy to conduct and proceed under mild conditions. Copyright
Generation and Rearrangement of 4aH-Carbazoles
Kulagowski, Janusz J.,Moody, Christopher J.,Rees, Charles W.
, p. 548 - 550 (2007/10/02)
Thermal and photochemical decomposition of benzotriazoles (3) gives carbazoles (4) and (5), and cyclopentaquinolines (6), the formation of these products being rationalised by rearrangements in 4aH-carbazole intermediates (7); one proposed intermediate (11c) has been intercepted in an extended cycloaddition reaction with acrylonitrile.
