26530-60-9 Usage
Description
Methyl 2-diMethoxyphosphorylpropanoate is an organic compound with the chemical structure featuring a phosphoryl group and a propanoate backbone. It is a key intermediate in the synthesis of various phosphonic acid derivatives and plays a significant role in the development of pharmaceuticals and other chemical products.
Uses
Used in Pharmaceutical Synthesis:
Methyl 2-diMethoxyphosphorylpropanoate is used as a key intermediate for the synthesis of tri-Me ether of phosphonoacetic acid, which is an important compound in the development of pharmaceuticals. The compound serves as a building block for creating more complex molecules with potential therapeutic applications.
Used in Chemical Research:
In the field of chemical research, Methyl 2-diMethoxyphosphorylpropanoate is utilized as a starting material for the synthesis of various phosphonic acid derivatives. These derivatives can be further explored for their potential applications in different industries, such as agriculture, materials science, and environmental science.
Used in Synthesis of Bioactive Molecules:
Methyl 2-diMethoxyphosphorylpropanoate is also used in the synthesis of bioactive molecules, which can be employed as potential therapeutic agents. The compound's unique chemical structure allows for the development of novel molecules with specific biological activities, contributing to the advancement of drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 26530-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,3 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26530-60:
(7*2)+(6*6)+(5*5)+(4*3)+(3*0)+(2*6)+(1*0)=99
99 % 10 = 9
So 26530-60-9 is a valid CAS Registry Number.
26530-60-9Relevant articles and documents
Neighbouring Phosphonate Group Participation in Carbene Chemistry
Tomioka, Hideo,Hirai, Katsuyuki
, p. 1611 - 1613 (2007/10/02)
Systematic studies of the effect of the neighbouring phosphonate group on the reactivities of carbene showed that the neighbouring phosphonate group exerts prominent effects on both the product distribution and the reaction products; the results are interpreted as indicating the extent of participation, which seems to be sensitive to the carbenic substituents.
