58816-03-8 Usage
Uses
Used in Coordination Chemistry:
(3,5-dimethylpyridin-4-yl)phosphonic acid is used as a chelating agent for forming stable complexes with metal ions. Its ability to bind with metals makes it a valuable component in various research and industrial applications.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, (3,5-dimethylpyridin-4-yl)phosphonic acid is utilized as a key intermediate in the synthesis of various drugs. Its unique structure allows for the development of new medicinal compounds with potential therapeutic benefits.
Used in Agrochemical Synthesis:
Similarly, in agrochemicals, (3,5-dimethylpyridin-4-yl)phosphonic acid serves as an important building block for the creation of effective pesticides and other agricultural products, contributing to enhanced crop protection and yield.
Used in Anti-cancer Research:
(3,5-dimethylpyridin-4-yl)phosphonic acid has been investigated for its potential anti-cancer properties, indicating its possible use in the development of novel cancer treatments. Its ability to target and affect cancer cells could lead to advancements in oncology.
Used in Anti-inflammatory Applications:
(3,5-dimethylpyridin-4-yl)phosphonic acid has also demonstrated anti-inflammatory potential, suggesting that it could be employed in the development of anti-inflammatory medications, which would be beneficial in treating a variety of inflammatory conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 58816-03-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,1 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58816-03:
(7*5)+(6*8)+(5*8)+(4*1)+(3*6)+(2*0)+(1*3)=148
148 % 10 = 8
So 58816-03-8 is a valid CAS Registry Number.
58816-03-8Relevant academic research and scientific papers
Preparation of pyridyl-4-phosphonates
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, (2008/06/13)
This invention relates to the preparation of pyridyl-4-phosphonates by reacting phosphite ester salts with pyridines which are N-substituted with sterically hindering or "bulky" groups such as "bulky" phenyl groups, for example trityl, φ3 C-.
