69796-30-1 Usage
Uses
Used in Flame Retardants Industry:
[hydroxy(4-hydroxyphenyl)methyl]phosphonic acid is used as a flame retardant additive for enhancing the fire resistance of various materials. Its phosphonic acid derivative nature contributes to the formation of a protective char layer, which helps slow down the combustion process and improve the overall safety of the treated materials.
Used in Metal Complex Agents Industry:
In the field of metal complex agents, [hydroxy(4-hydroxyphenyl)methyl]phosphonic acid serves as a crucial component in the development of chelating agents. These agents are essential for stabilizing metal ions in various chemical processes, thus improving the efficiency and performance of the reactions involving metal complexes.
Used in Corrosion Inhibition:
[hydroxy(4-hydroxyphenyl)methyl]phosphonic acid is employed as a corrosion inhibitor in the protection of metals from degradation due to environmental factors. Its ability to form a protective film on metal surfaces helps in reducing the rate of corrosion, thereby extending the lifespan of the materials and structures.
Used in Pharmaceutical Synthesis:
[hydroxy(4-hydroxyphenyl)methyl]phosphonic acid is utilized in the synthesis of various pharmaceuticals, where its unique structure and functional groups play a vital role in the development of new drugs. The hydroxy and phenolic groups in [hydroxy(4-hydroxyphenyl)methyl]phosphonic acid enable it to form stable complexes with biologically active molecules, making it a valuable intermediate in drug design and synthesis.
Used in Agrochemicals Synthesis:
Similarly, in the agrochemicals industry, [hydroxy(4-hydroxyphenyl)methyl]phosphonic acid is used as a key intermediate in the synthesis of various agrochemicals, such as pesticides and herbicides. Its ability to form stable complexes with target molecules allows for the development of more effective and targeted agrochemicals.
Used in Antimicrobial Applications:
[hydroxy(4-hydroxyphenyl)methyl]phosphonic acid has been studied for its potential antibacterial and antiviral properties. Its phosphonic acid derivative nature may contribute to its ability to disrupt bacterial cell walls and inhibit viral replication, making it a promising candidate for the development of new antimicrobial agents.
Check Digit Verification of cas no
The CAS Registry Mumber 69796-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,7,9 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69796-30:
(7*6)+(6*9)+(5*7)+(4*9)+(3*6)+(2*3)+(1*0)=191
191 % 10 = 1
So 69796-30-1 is a valid CAS Registry Number.
69796-30-1Relevant academic research and scientific papers
Boduszek, Bogdan,Halama, Agnieszka
, p. 151 - 158 (1998)
α-Aminobenzylphosphonic acids possessing the hydroxy groups in ortho and para positions, underwent a C-P bond cleavage during heating with aqueous NaOH solution. In the case of o- and p-hydroxy diethyl esters 1 and 3 the products of the cleavage were the corresponding aldehydes and phosphorous acid (H3PO3). The m-hydroxy derivative was not affected by a base. It has been found, that displacement of the hydroxy group by the methoxy one in the p-hydroxybenzyl(α-amino)phosphonic acid leads to a stability of such a compound towards a base; no a C-P bond cleavage was observed in this case.
