1912-16-9 Usage
Description
Pyridine, 2-methyl-4,6-diphenylis a chemical compound with the molecular formula C20H17N. It is a derivative of pyridine, a six-membered aromatic ring with one nitrogen atom. Pyridine, 2-methyl-4,6-diphenylis characterized by a methyl group at the 2-position and two phenyl groups at the 4and 6-positions.
Uses
Used in Organic Synthesis:
Pyridine, 2-methyl-4,6-diphenylis used as a building block for various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it an important intermediate for the production of numerous complex compounds.
Used in Pharmaceutical Industry:
Pyridine, 2-methyl-4,6-diphenylis used as a key intermediate in the synthesis of various pharmaceuticals due to its unique structure and reactivity.
Used in Agrochemical Industry:
Pyridine, 2-methyl-4,6-diphenylis used as a building block in the development of agrochemicals, contributing to the production of effective and targeted products.
Used in Chemical Processes:
Pyridine, 2-methyl-4,6-diphenylis used as a solvent and chemical reagent in various chemical processes, facilitating reactions and improving process efficiency.
Used in Research and Development:
Pyridine, 2-methyl-4,6-diphenylis being researched for potential pharmacological applications due to its biological properties, offering opportunities for the discovery of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 1912-16-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1912-16:
(6*1)+(5*9)+(4*1)+(3*2)+(2*1)+(1*6)=69
69 % 10 = 9
So 1912-16-9 is a valid CAS Registry Number.
1912-16-9Relevant articles and documents
A New Pyridine Synthesis
Kelly, T. Ross,Liu, Hshiou-ting
, p. 4998 - 4999 (1985)
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NH4I-Triggered [4 + 2] Annulation of α,β-Unsaturated Ketoxime Acetates with N-Acetyl Enamides for the Synthesis of Pyridines
Duan, Jindian,Zhang, Lei,Xu, Gaochen,Chen, Heming,Ding, Xiaojuan,Mao, Yiyang,Rong, Binsen,Zhu, Ning,Guo, Kai
, p. 8157 - 8165 (2020/07/25)
The NH4I-triggered formal [4 + 2] annulation of α,β-unsaturated ketoxime acetates with N-acetyl enamides has been developed. The current protocol employs electron-rich enamides as C2 synthons and enables the efficient and straightforward construction of polysubstituted pyridines in moderate to good yields based on metal-free systems. The reaction tolerates a wide range of functional groups and represents an alternate route toward the synthesis of pyridine derivatives.
Gao, Qinghe,Yan, Huijuan,Wu, Manman,Sun, Jiajia,Yan, Xiqing,Wu, Anxin
, p. 2342 - 2348 (2018/04/05)
