869642-36-4 Usage
Uses
Used in Organic Synthesis:
9H-Carbazol-1-ylboronic acid is used as a building block for the synthesis of various functionalized carbazole derivatives. Its unique structure allows for the creation of a wide range of compounds with diverse properties, making it valuable in the development of new organic materials.
Used in Materials Science:
In the field of materials science, 9H-Carbazol-1-ylboronic acid is utilized in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics. Its incorporation into these technologies can enhance their performance and efficiency, contributing to advancements in display and energy conversion technologies.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
9H-Carbazol-1-ylboronic acid is used as a reagent in Suzuki-Miyaura cross-coupling reactions, a class of palladiumor nickel-catalyzed carbon-carbon bond forming reactions. This application is crucial for the synthesis of complex organic molecules and the formation of new chemical entities in pharmaceutical and chemical research.
Overall, 9H-Carbazol-1-ylboronic acid is a versatile and important compound with potential uses in various fields of chemistry and materials science, including the synthesis of functionalized carbazole derivatives, the development of advanced materials for electronic devices, and as a key reagent in cross-coupling reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 869642-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,6,4 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 869642-36:
(8*8)+(7*6)+(6*9)+(5*6)+(4*4)+(3*2)+(2*3)+(1*6)=224
224 % 10 = 4
So 869642-36-4 is a valid CAS Registry Number.
869642-36-4Relevant academic research and scientific papers
Phosphorescence host material and application thereof in organic electroluminescence devices
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Paragraph 0102; 0104; 0105-0107, (2019/10/15)
The invention relates to an organic compound; the organic compound is as shown in a formula (1), and the formula (1) is described in the description, wherein the dotted circle represents a benzene ring structure, and indole derivative groups positioned at the two sides of the benzene ring structure are fused into indolocarbazole derivatives by means of the benzene ring structure; X1-X8 is CR or N;one of Ar1 and Ar2 is selected from pi-absence electron-type aromatic groups of C3-C30; R is selected from hydrogen, aliphatic hydrocarbon groups of C1-C4, aryl groups of C6-C30 and heteroaryl groupsof C3-C30; when multiple Rs exist, all the Rs can be the same or different; m and n are respectively integers within a range of 1-4; p is 1 or 2; L1 and L2 are respectively and independently selectedfrom a single bond, arylene groups of C6-C12 or hetero-arylene groups of C3-C12; when substituents exist in the groups, the substituents are respectively and independently selected from halogen, alkyl or cycloalkyl groups of C1-C10, alkenyl or cycloalkenyl groups of C2-C6, alkoxy or thioalkoxy groups of C1-C6, monocyclic aryl or fused ring aryl groups of C6-C30, monocyclic heteroaryl or fused ring heteroaryl groups of C3-C30, or a combined structure of the groups.
