1001911-63-2 Usage
Description
(9-phenyl-9H-carbazol-2-yl)boronic acid is an organic compound with the molecular formula C16H13BO2. It is characterized by its boron atom bonded to a phenyl group and a carbazole ring, which gives it unique chemical properties and reactivity. (9-phenyl-9H-carbazol-2-yl)boronic acid is known for its potential applications in various fields due to its structural features and reactivity.
Uses
Used in Organic Synthesis:
(9-phenyl-9H-carbazol-2-yl)boronic acid is used as an intermediate in organic synthesis for the development of new compounds with specific properties and functions. Its unique structure allows it to participate in various chemical reactions, making it a valuable building block in the synthesis of complex organic molecules.
Used in Laboratory Research and Development:
In the field of laboratory research and development, (9-phenyl-9H-carbazol-2-yl)boronic acid is utilized to explore its chemical properties, reactivity, and potential applications in creating new materials and compounds. Researchers can use this compound to study its interactions with other molecules and to develop new synthetic routes for the production of novel organic compounds.
Used in Chemical and Pharmaceutical Synthesis:
(9-phenyl-9H-carbazol-2-yl)boronic acid is also used in the chemical and pharmaceutical industries for the synthesis of various products. Its unique structure and reactivity make it a valuable component in the development of new drugs, materials, and other chemical products. The compound can be employed in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals, contributing to the advancement of these industries.
Synthesis
Sub 1-3-1 (6.4g, 20mmol) was dissolved in anhydrous Ether, lowering the temperature of the reaction to -78°C, n-BuLi (2.5M in hexane) (1.4g, 22mmol) was added dropwise slowly, and after, the reaction It was stirred for 30 minutes. After lowering the temperature of the reaction back to -78°C dropwise Triisopropyl borate (5.6g, 30mmol). Stirring at room temperature, diluted with water and it binds the 2N HCl. After completion of reaction, ethyl acetate and water, dried over MgSO4 and the organic layer was extracted and recrystallized silicagel column and the resulting organic material and then concentrated to a Sub 1-4-1 4.5g (yield: 78%) was obtained.
Check Digit Verification of cas no
The CAS Registry Mumber 1001911-63-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,1,9,1 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1001911-63:
(9*1)+(8*0)+(7*0)+(6*1)+(5*9)+(4*1)+(3*1)+(2*6)+(1*3)=82
82 % 10 = 2
So 1001911-63-2 is a valid CAS Registry Number.
1001911-63-2Relevant articles and documents
Color-tunable thiazole-based iridium(III) complexes: Synthesis, characterization and their OLED applications
Chau, Nga-Yuen,Ho, Po-Yu,Ho, Cheuk-Lam,Ma, Dongge,Wong, Wai-Yeung
, p. 92 - 100 (2017)
With respect to the commonly used electron-deficient pyridyl group in the benchmark dopant Ir(ppy)3, incorporating the electron-rich thiazolyl group with different chromophores have not been extensively studied. In this paper, some iridium(III) complexes bearing functional ligands with the thiazolyl moiety were synthesized and characterized by1H and13C NMR, UV–Vis absorption and photoluminescence spectroscopy. The emission color of these thiazole-based Ir(III) complexes can be tuned from yellow to red and the best phosphorescent organic light-emitting device exhibited the maximum external quantum efficiency of 11.1%, current efficiency of 35.8 cd/A and power efficiency of 21.9 lm/W.
Compound constituting a hole transfer layer and an electron transfer layer of an organic light emitting diode or a method for producing the same
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Paragraph 0089-0100, (2020/09/16)
The present invention relates to a compound constituting a hole transport layer and an electron transport layer of an organic light emitting diode, or a method for manufacturing the same. According to the present invention, it is possible to provide a plurality of compounds having excellent yields and excellent purity constituting the hole transport layer and the electron transport layer. An object of the present invention is to provide the compound constituting the hole transport layer and the electron transport layer of the organic light emitting diode, or the method for manufacturing the same.(AA) HPLC analysis result of a final productCOPYRIGHT KIPO 2020
An organic electroluminescent element using this derivative bis carbazole
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Paragraph 0171-0173, (2020/10/21)
PROBLEM TO BE SOLVED: To provide a biscarbazole derivative capable of improving emission efficiency and an emission life of an organic electroluminescence element, and to provide an organic electroluminescence element using the derivative.SOLUTION: The biscarbazole derivative is represented by the formula.