882864-93-9 Usage
Uses
Used in Coordination Chemistry:
N,N-dimethyl-3,3'-bipyridin-6-amine is used as a ligand for the synthesis of coordination complexes, leveraging its ability to bind with metal ions to form stable complexes with potential applications in various fields.
Used in Catalysis:
N,N-dimethyl-3,3'-bipyridin-6-amine serves as a catalyst or a catalyst precursor, where its coordination properties facilitate chemical reactions, enhancing their efficiency and selectivity.
Used in Pharmaceutical Production:
N,N-dimethyl-3,3'-bipyridin-6-amine is utilized in the development of pharmaceuticals, contributing to the synthesis of active pharmaceutical ingredients or serving as a key intermediate in drug synthesis.
Used in Agrochemicals:
In the agrochemical industry, N,N-dimethyl-3,3'-bipyridin-6-amine is applied in the production of pesticides or other agrochemicals, where its coordination chemistry can be harnessed to improve the effectiveness of these products.
Used in Dyes:
N,N-dimethyl-3,3'-bipyridin-6-amine is also used in the formulation of dyes, where its electronic properties and ability to form complexes can influence color and stability.
Used in Materials Science:
N,N-dimethyl-3,3'-bipyridin-6-amine has potential applications in materials science, where its coordination abilities and electronic properties are of interest for the development of new functional materials, such as metal-organic frameworks and other advanced materials with specific properties for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 882864-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,8,6 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 882864-93:
(8*8)+(7*8)+(6*2)+(5*8)+(4*6)+(3*4)+(2*9)+(1*3)=229
229 % 10 = 9
So 882864-93-9 is a valid CAS Registry Number.
882864-93-9Relevant academic research and scientific papers
Synthesis of biaryls through a one-pot tandem borylation/Suzuki-Miyaura cross-coupling reaction catalyzed by a palladacycle
Wang, Lianhui,Cui, Xiuling,Li, Jingya,Wu, Yusheng,Zhu, Zhiwu,Wu, Yangjie
experimental part, p. 595 - 603 (2012/03/09)
The tricyclohexylphosphane adduct of cyclopalladated ferrocenylimine I exhibited high catalytic activity in the one-pot borylation/Suzuki-Miyaura coupling (BSC) reaction with low catalyst loading (2 mol-%). Various biaryls were obtained in good to excellent yields for 37 examples. This process was applied to aryl and heteroaryl halides (Br and Cl) containing a variety of functional groups and did not require an excess amount of phosphane ligand and the addition of the palladium catalyst in the second step. Cyclopalladated ferrocenylimine I exhibited high catalytic activity in the borylation/Suzuki- Miyaura coupling (BSC) reaction with low catalyst loading. Various unsymmetrical biaryls were obtained ingood to excellent yields in one pot. This protocol was applied to aryl and heteroaryl halides (Br and Cl) containing a variety of functional groups without adding catalyst in the second step. Copyright
