793681-93-3 Usage
Uses
Used in Organic Synthesis:
9H-Carbazole, 9-octyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)is used as a key intermediate in organic synthesis for the preparation of various functionalized carbazole derivatives. Its boron-containing group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of diverse carbazole-based compounds with potential applications in different fields.
Used in Organic Electronic Devices:
In the field of materials science, 9H-Carbazole, 9-octyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)is utilized in the development of organic electronic devices. Its incorporation into the molecular structure of these devices enhances their performance and efficiency.
Used in Organic Light-Emitting Diodes (OLEDs):
9H-Carbazole, 9-octyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)is used as a component in the design and synthesis of organic light-emitting diodes (OLEDs). Its presence in the molecular structure of OLEDs contributes to improved light emission properties, such as brightness, color, and efficiency.
Used in Organic Photovoltaics (OPVs):
In the renewable energy sector, 9H-Carbazole, 9-octyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)is employed in the development of organic photovoltaics (OPVs). Its integration into the molecular structure of OPVs enhances their photovoltaic performance, leading to increased power conversion efficiency and overall energy output.
Used in Pharmaceutical Industry:
9H-Carbazole, 9-octyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)can be used as a starting material for the synthesis of carbazole-based pharmaceutical compounds. Its unique structure and functional groups make it a promising candidate for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, 9H-Carbazole, 9-octyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)serves as a valuable model compound for studying the properties and reactivity of carbazole derivatives. Its use in research helps to advance the understanding of the structure-property relationships in this class of compounds and facilitates the discovery of new applications and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 793681-93-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,3,6,8 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 793681-93:
(8*7)+(7*9)+(6*3)+(5*6)+(4*8)+(3*1)+(2*9)+(1*3)=223
223 % 10 = 3
So 793681-93-3 is a valid CAS Registry Number.
793681-93-3Relevant academic research and scientific papers
Novel BODIPY dyes with electron donor variety for dye-sensitized solar cells
Liao, Junxu,Zhao, Hongbin,Xu, Yongjun,Zhou, Weinan,Peng, Fei,Wang, Yong,Fang, Yutang
, p. 33975 - 33985 (2017/07/17)
Four new donor-π-acceptor (D-π-A) structured organic sensitizers (CB1-4), with N-octyl or N-methoxyphenyl carbazole connected to a 2-cyanoacrylate BODIPY module through their 2 or 3-positions, were designed and synthesized for application in dye-sensitize
Novel 2,6-site-substituted BODIPY organic dye sensitizer and preparation method therefor
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Paragraph 0078; 0079; 0082; 0083, (2016/10/09)
The present invention relates to a novel 2,6-site-substituted BODIPY organic dye sensitizer and a preparation method therefor. The organic dye sensitizer is organic photovoltaic materials with a D-pi-A structure. By taking a meso-site-substituted BODIPY core as a pi bridge framework, the sites 2 and 6 of the BODIPY core is respectively substituted by an electron donor and an electron acceptor. The present invention further discloses a preparation method for the above the dye sensitizer. The preparation method obtains a dye molecule having a general structural formula I by taking 2,4-dimethylpyrrole as an initial reaction raw material, performing a serials of simple synthesis reactions, and finally performing classical Suzuki coupling and Knoevenagel condensation reactions. The dye sensitizer synthesis method is simple, easy to control and high in yield, and has general applicability. When the method is applied to dye sensitized solar cell preparation, a dye sensitized solar cell material with a high fill factor and an ideal photoelectric conversion efficiency can be obtained. The formula I is shown in the description.
Improved photovoltaic performance of star-shaped molecules with a triphenylamine core by tuning the substituted position of the carbazolyl unit at the terminal
Zhou, Pei,Dang, Dongfeng,Xiao, Manjun,Wang, Qiong,Zhong, Juan,Tan, Hua,Pei, Yong,Yang, Renqiang,Zhu, Weiguo
supporting information, p. 10883 - 10889 (2015/05/27)
Two star-shaped molecules of TPA(BT-2Cz)3 and TPA(BT-3Cz)3 with a triphenyl-amine (TPA) core were designed and synthesized, in which 2- and 3-carbazolyl units (2Cz and 3Cz) are attached to the benzothiadiazole (BT) arms as planar ter
