71172-56-0 Usage
Structure
A pyridine derivative with a methyl group and a methoxyethyl group attached to the pyridine ring.
Usage
Commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals.
Application
Utilized as a solvent in organic synthesis and as an intermediate in the production of various industrial chemicals.
Versatility
The chemical properties of 2-(2-methoxyethyl)-6-methylpyridine make it a valuable and useful compound in a wide range of applications, particularly in the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 71172-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,1,7 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71172-56:
(7*7)+(6*1)+(5*1)+(4*7)+(3*2)+(2*5)+(1*6)=110
110 % 10 = 0
So 71172-56-0 is a valid CAS Registry Number.
71172-56-0Relevant academic research and scientific papers
Ogiwara, Yohei,Kochi, Takuya,Kakiuchi, Fumitoshi
, p. 3254 - 3257 (2011)
Catalytic conversion of unreactive sp3 C-O bonds in alkyl ethers to C-C bonds is described. Alkyl ethers bearing 2- or 4-pyridyl groups were coupled with triarylboroxines in the presence of a ruthenium catalyst. Triarylboroxines bearing a variety of functional groups including electron-withdrawing and -donating groups can be used for the reaction. No additional base was required for the coupling with the organoboron reagents, and base-sensitive groups can be tolerated. The reaction is considered to proceed via dehydroalkoxylation followed by addition of triarylboroxines to form C-C bonds.
