330792-75-1 Usage
Description
N-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is a boronic acid derivative that serves as a versatile building block in organic synthesis, particularly for the development of pharmaceuticals, agrochemicals, and materials science. This chemical compound features a phenyl group attached to a boron-containing aniline molecule, which endows it with the ability to form stable complexes with other organic molecules, making it a valuable intermediate in a variety of chemical reactions.
Uses
Used in Pharmaceutical Industry:
N-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is used as a key intermediate in the synthesis of complex organic molecules for pharmaceutical applications. Its boron-containing structure facilitates the formation of stable complexes, which is crucial for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical sector, N-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is utilized as a building block for the creation of novel agrochemicals. Its ability to form stable complexes with other organic molecules aids in the development of more effective and targeted pesticides and other agricultural chemicals.
Used in Materials Science:
N-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is employed as a precursor in the synthesis of advanced materials with unique properties. Its boron-containing structure allows for the formation of stable complexes, which can be leveraged to create materials with enhanced performance characteristics.
Used in Suzuki-Miyaura Coupling Reactions:
N-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline plays a significant role in Suzuki-Miyaura coupling reactions, a widely used method for the synthesis of complex organic molecules. As a boronic acid derivative, it readily participates in these cross-coupling reactions, enabling the formation of carbon-carbon bonds and the construction of diverse molecular architectures.
Check Digit Verification of cas no
The CAS Registry Mumber 330792-75-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,7,9 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 330792-75:
(8*3)+(7*3)+(6*0)+(5*7)+(4*9)+(3*2)+(2*7)+(1*5)=141
141 % 10 = 1
So 330792-75-1 is a valid CAS Registry Number.
330792-75-1Relevant articles and documents
Unreactive C-N Bond Activation of Anilines via Photoinduced Aerobic Borylation
Ji, Shuohan,Qin, Shengxiang,Yin, Chunyu,Luo, Lu,Zhang, Hua
supporting information, p. 64 - 68 (2021/12/27)
Unreactive C-N bond activation of anilines was achieved by photoinduced aerobic borylation. A diverse range of tertiary and secondary anilines were converted to aryl boronate esters in moderate to good yields with wide functional group tolerance under simple and ambient photochemical conditions. This transformation achieved the direct and facile C-N bond activation of unreactive anilines, providing a convenient and practical route transforming widely available anilines into useful aryl boronate esters.
Organic electroluminescent material and device thereof
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Paragraph 0146-0149, (2020/09/30)
Disclosed are an organic electroluminescent material and a device thereof. The organic electroluminescent material is a triaryl amine-carbazole quinazoline compound substituted by a novel fluorenyl group and an analogue structural unit thereof. The compound is used as a host material in an electroluminescent device and provides a better device performance.
Anti-1,2,2,3,4,4-hexamethylphosphetane 1-oxide
Nykaza, Trevor V.,Cooper, Julian C.,Radosevich, Alexander T.
, p. 418 - 435 (2019/11/21)
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