1245646-00-7 Usage
Uses
Used in Coordination Chemistry:
2'-methoxy-N-methyl-4,4'-bipyridin-2-amine is used as a ligand for forming coordination complexes with metal ions. Its ability to chelate with metal ions makes it a valuable component in the synthesis of coordination compounds, which have applications in various fields such as catalysis, medicine, and materials science.
Used in Organic Synthesis:
In the realm of organic synthesis, 2'-methoxy-N-methyl-4,4'-bipyridin-2-amine serves as a key intermediate or building block for the creation of more complex organic molecules. Its presence of methoxy and methyl groups allows for further functionalization and the synthesis of a wide range of organic compounds.
Used in Materials Science:
2'-methoxy-N-methyl-4,4'-bipyridin-2-amine is utilized in materials science for the development of functional materials. 2'-methoxy-N-methyl-4,4'-bipyridin-2-amine's structural features, including the methoxy and methyl groups, contribute to the properties of the resulting materials, making it suitable for applications in areas such as sensors, catalysts, and advanced materials with specific electronic or optical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1245646-00-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,6,4 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1245646-00:
(9*1)+(8*2)+(7*4)+(6*5)+(5*6)+(4*4)+(3*6)+(2*0)+(1*0)=147
147 % 10 = 7
So 1245646-00-7 is a valid CAS Registry Number.
1245646-00-7Relevant 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
