38840-06-1 Usage
Uses
Used in Chemical Research:
4-Methyl-3,3'-bipyridine is used as a ligand in chemical research for its ability to bind with metal ions, facilitating the study of various chemical reactions and processes. Its structure allows it to donate two pairs of electrons to metal ions, which is essential for understanding the properties and behavior of metal complexes.
Used in Inorganic Chemistry:
In inorganic chemistry, 4-methyl-3,3'-bipyridine is utilized as a ligand to form transition metal complexes, which are crucial for investigating the properties and reactivity of these complexes in various chemical systems.
Used in Biochemistry:
4-Methyl-3,3'-bipyridine is also used in biochemistry to study the interactions between metal ions and biological molecules, such as enzymes and proteins, providing insights into the role of metal ions in biological processes.
Used in Industrial Production:
4-methyl-3,3'-bipyridine is industrially produced and used in the synthesis of various chemical products, taking advantage of its properties as a ligand and its solubility characteristics in organic solvents.
Check Digit Verification of cas no
The CAS Registry Mumber 38840-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,4 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38840-06:
(7*3)+(6*8)+(5*8)+(4*4)+(3*0)+(2*0)+(1*6)=131
131 % 10 = 1
So 38840-06-1 is a valid CAS Registry Number.
38840-06-1Relevant 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
