1072933-64-2 Usage
Uses
Used in Pharmaceutical Synthesis:
3-Methoxy-5-(2-methyl-1,3-dioxolan-2-yl)pyridine is used as a key intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into complex molecular structures, enhancing the development of new drugs with improved therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, 3-Methoxy-5-(2-methyl-1,3-dioxolan-2-yl)pyridine is utilized as a precursor in the creation of pesticides and other agrochemicals, contributing to the development of more effective and targeted crop protection agents.
Used in Organic Compounds Production:
As an intermediate, 3-Methoxy-5-(2-methyl-1,3-dioxolan-2-yl)pyridine is employed in the production of a variety of organic compounds, leveraging its unique structure and reactivity to form new molecules with specific applications in various fields.
Used in Drug Design and Bioactive Molecule Development:
3-Methoxy-5-(2-methyl-1,3-dioxolan-2-yl)pyridine is used as a building block in drug design, allowing researchers to explore its potential biological activities and incorporate it into the development of innovative drugs and bioactive molecules for treating various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 1072933-64-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,2,9,3 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1072933-64:
(9*1)+(8*0)+(7*7)+(6*2)+(5*9)+(4*3)+(3*3)+(2*6)+(1*4)=152
152 % 10 = 2
So 1072933-64-2 is a valid CAS Registry Number.
1072933-64-2Relevant academic research and scientific papers
Palladium-catalyzed regiocontrolled internal heteroarylation of electron-rich olefins with heteroaryl halides
Xu, Dan,Liu, Zhihua,Tang, Weijun,Xu, Lijin,Hyder, Zeynab,Xiao, Jianliang
scheme or table, p. 6104 - 6107 (2009/04/04)
A highly efficient palladium-catalyzed Heck coupling reaction of heteroaryl halides with electron-rich vinyl ether and hydroxyalkyl vinyl ethers is described. It was found that the choice of solvent, ligand, and reaction temperature had a fundamental influence on the regioselectivity and reactivity of the reaction, and the combination of Pd(OAc)2 and DPPF in ethylene glycol led to the most effective catalytic system. Under these conditions, a variety of heteroaryl halides reacted very quickly with electron-rich olefins to afford exclusively the branched products in good to excellent yields without employing triflates, halide scavengers, or ionic liquids.
