21064-50-6 Usage
Chemical class
Belongs to the class of benzo[c]carbazoles, which are polycyclic aromatic hydrocarbons.
Synthetic compound
It is a synthetic compound, not found naturally.
Potential applications
Has potential applications in the field of organic electronics and optoelectronics.
Semiconductor material
Studied for its ability to act as a semiconductor material in organic photovoltaic cells and organic light emitting diodes.
Chemical structure
Consists of a fused benzo ring system with a methyl group attached at the 10th position.
Electronic and optical properties
Researched for its potential to exhibit interesting electronic and optical properties.
Compound of interest
It is a compound of interest for its potential applications in advanced materials and devices in the field of organic electronics.
Check Digit Verification of cas no
The CAS Registry Mumber 21064-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,6 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21064-50:
(7*2)+(6*1)+(5*0)+(4*6)+(3*4)+(2*5)+(1*0)=66
66 % 10 = 6
So 21064-50-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H13N/c1-11-6-8-15-14(10-11)17-13-5-3-2-4-12(13)7-9-16(17)18-15/h2-10,18H,1H3
21064-50-6Relevant articles and documents
One-pot synthesis of carbazoles via tandem C-C cross-coupling and reductive amination
Goo, Deuk-Young,Woo, Sang Kook
supporting information, p. 122 - 130 (2015/12/30)
We have developed a highly efficient synthetic route to carbazoles that employs sequential C-C/C-N bond formation via Suzuki cross-coupling and Cadogan cyclization using commercially available or easily preparable starting materials. The developed method is compatible with electron neutral, rich or deficient substrates. The synthetic utility of this method was demonstrated by the concise syntheses of four natural products (glycozoline, glycozolicine, glycozolidine and clausenalene).
Acid-catalyzed rearrangement of diaryl hydrazides for the efficient synthesis of functionalized 2,2′-diamino-1,1′-biaryls
Lim, Young-Kwan,Jung, Jin-Woo,Lee, Haiwon,Cho, Cheon-Gyu
, p. 5778 - 5781 (2007/10/03)
Diaryl hydrazides prepared from the Pd(0)- or Cu(I)-catalyzed coupling reactions of aryl hydrazides and aryl halides underwent the acid-catalyzed rearrangements to a series of previously unknown 2,2′-diaminobiaryls in good overall yields. The mildness of the reaction conditions allows the presence of various functional groups.
