Indolocarbazoles
Indolocarbazoles are a class of organic compounds that possess a unique structural feature consisting of an indole ring fused to a carbazole moiety. These molecules exhibit significant potential in various applications due to their interesting electronic properties and versatile structure. Indolocarbazoles have been extensively studied for use in organic electronics, particularly in the fabrication of organic light-emitting diodes (OLEDs). Their ability to incorporate both aromatic electron-donating indole and electron-accepting carbazole groups makes them valuable for designing materials with tunable properties suitable for different device requirements. Additionally, they are explored in photovoltaics, sensors, and as potential pharmaceutical agents due to their chemical diversity and structural flexibility. The synthesis of indolocarbazoles can be achieved through various methods including multistep organic reactions and cross-coupling strategies, allowing for the introduction of a wide range of functional groups.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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Arcyriaflavin A | 118458-54-1 | C20H11N3O2 |
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5H-Indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione,1-chloro-13-[6-O-[2,4-dideoxy-4-(methylamino)-a-L-threo-pentopyranosyl]-4-O-methyl-b-D-glucopyranosyl]-12,13-dihydro-6-methyl- | 102644-20-2 | C34H35ClN4O9 |
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K 252 | 97161-97-2 | C27H21N3O5 |
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K-252b | 99570-78-2 | C26H19N3O5 |
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Rebeccamycin | 93908-02-2 | C27H21Cl2N3O7 |
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5H-Indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione,1,11-dibromo-12,13-dihydro-12-(4-O-methyl-b-D-glucopyranosyl)- | 137605-02-8 | C27H21Br2N3O7 |
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THK01 | 2226941-26-8 | C20H13N3O2 |
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Staurosporine; 4'-N-Formyl | 161973-03-1 | C29H26N4O4 |
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Staurosporine; 5'α-Hydroxy | 308847-74-7 | C28H26N4O4 |
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Staurosporine; 11-Hydroxy, 4'-N-de-Me | 272766-45-7 | C27H24N4O4 |
Related Literature
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Dhamodaran Manikandan,S. Amirthapandian,I. S. Zhidkov,A. I. Kukharenko,S. O. Cholakh,Ramaswamy Murugan Phys. Chem. Chem. Phys., 2018,20, 6500-6514
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Bo Cao,Yin Wei Chem. Commun., 2018,54, 2870-2873
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Yu-Nong Li,Liang-Nian He,Xian-Dong Lang,Xiao-Fang Liu,Shuai Zhang RSC Adv., 2014,4, 49995-50002
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Cheng Fang,Jinjian Wu,Zahra Sobhani,Md. Al Amin,Youhong Tang Anal. Methods, 2019,11, 163-170
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Eunice Y.-L. Hui,Bhimsen Rout,Yaw Sing Tan,Kok-Ping Chan,Charles W. Johannes Org. Biomol. Chem., 2018,16, 389-392
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