883-39-6 Usage
Description
1-Phenyl-1H-benzotriazole is an organic compound that belongs to the class of benzotriazoles. It is characterized by the presence of a phenyl group attached to a benzotriazole core, which provides unique chemical properties and reactivity. This versatile molecule is known for its ability to form stable complexes with metal ions, making it a valuable component in various chemical reactions and applications.
Uses
Used in Chemical Synthesis:
1-Phenyl-1H-benzotriazole is used as a reagent in the preparation of possible surrogates for Kobayashi's aryne precursors. Its ability to form stable complexes with metal ions allows it to facilitate the synthesis of these precursors, which are important intermediates in organic chemistry for the formation of various complex organic molecules.
Used in Catalysts and Ligands:
Due to its strong affinity for metal ions, 1-Phenyl-1H-benzotriazole is employed as a ligand in the development of homogeneous catalysts. These catalysts are used to accelerate chemical reactions, improving their efficiency and selectivity. The benzotriazole moiety in this compound contributes to the stability and performance of the resulting catalysts.
Used in Corrosion Inhibition:
1-Phenyl-1H-benzotriazole is also utilized as a corrosion inhibitor in various industries, such as the automotive and aerospace sectors. Its ability to form stable complexes with metal ions helps protect metal surfaces from corrosion, extending the lifespan of components and reducing maintenance costs.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-Phenyl-1H-benzotriazole is used as a building block for the synthesis of various drug candidates. Its unique chemical properties and reactivity make it a valuable component in the development of new medications with potential therapeutic applications.
Used in Materials Science:
1-Phenyl-1H-benzotriazole is employed in the development of advanced materials, such as organic semiconductors and conductive polymers. Its electronic properties and ability to form stable complexes with metal ions contribute to the performance and stability of these materials, which have potential applications in electronic devices, sensors, and energy storage systems.
Check Digit Verification of cas no
The CAS Registry Mumber 883-39-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 883-39:
(5*8)+(4*8)+(3*3)+(2*3)+(1*9)=96
96 % 10 = 6
So 883-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H9N3/c1-2-6-10(7-3-1)15-12-9-5-4-8-11(12)13-14-15/h1-9H
883-39-6Relevant articles and documents
Synthesis of functionized N-arylbenzotriazoles via palladium catalyzed intramolecular amination
Gan, Xiaoting,Shu, Hanyu,Wang, Dachao,Zhou, Jun,Zhou, Lewei
supporting information, (2021/12/29)
The functionalized benzotriazoles are prepared by palladium catalyzed intramolecular amination of 2-bromodiaryltriazene. By screening the reaction conditions, such as ligand, solvent, base and reaction concentration, the optimal reaction conditions were o
L-Proline N-oxide dihydrazides as an efficient ligand for cross-coupling reactions of aryl iodides and bromides with amines and phenols
Ding, Zhiqiang,Nie, Nan,Chen, Tian,Meng, Lingxin,Wang, Gongshu,Chen, Zhangpei,Hu, Jianshe
supporting information, (2020/12/21)
A novel catalytic system based on L-proline N-oxide/CuI was developed and applied to the cross-coupling reactions of various N- and O- nucleophilic reagents with aryl iodides and bromides. This strategy featured in the employment of an-proline derived dihydrazides N-oxide compound as the superior supporting ligand. By using this protocol, a variety of products, including N-arylimidazoles, N-arylpyrazoles, N-arylpyrroles, N-arylamines, and aryl ethers, were synthesized with up to 99% yield.
Cu-catalyzed arylation of 1-acyl-1H-1,2,3-Benzotriazoles via C–N activation
Zhang, Wenying,Wang, Yangyang,Jia, Xiangru,Du, Zhengyin,Fu, Ying
, p. 64 - 67 (2019/06/10)
An efficient copper-catalyzed arylation reaction of 1-acyl-1H-1,2,3-benzotriazoles with diaryliodonium salts via C–N activation is explored. The reaction is conducted regioselectively to form 1-aryl-1H-1,2,3-benzotriazoles in MeCN at 80 °C in the presence of cesium carbonate. 29 examples are given with the product yield of up to 84%. The probable reaction mechanism is proposed.
