7252-14-4 Usage
Description
[hydroxy(phenyl)methyl]phosphonic acid is a chemical compound that features a phosphonic acid group connected to a hydroxy(phenyl)methyl group. [hydroxy(phenyl)methyl]phosphonic acid is known for its potential interactions with biological systems due to the presence of the hydroxy group, making it a subject of interest in medicinal and pharmacological research. It also plays a role in organic synthesis and serves as a building block for creating complex molecules.
Uses
Used in Water Treatment:
[hydroxy(phenyl)methyl]phosphonic acid is used as a corrosion inhibitor to prevent the deterioration of metal surfaces in water treatment systems. Its application helps to extend the lifespan of equipment and infrastructure, reducing maintenance costs and downtime.
Used in Metal Ion Sequestration:
As a chelating agent, [hydroxy(phenyl)methyl]phosphonic acid is employed to sequester metal ions, which can be crucial in various industrial processes. By binding to metal ions, it helps to control their reactivity and prevent unwanted side reactions, ensuring process efficiency and product quality.
Used in Flame Retardancy:
[hydroxy(phenyl)methyl]phosphonic acid has been investigated for its potential use as a flame retardant, adding fire resistance to materials and products. This application can be particularly valuable in industries where safety and prevention of fire hazards are paramount.
Used in Pharmaceutical Formulations:
[hydroxy(phenyl)methyl]phosphonic acid's potential interactions with biological systems make [hydroxy(phenyl)methyl]phosphonic acid an interesting candidate for use in pharmaceutical formulations. It may be utilized in the development of new drugs or as a component in existing medications, contributing to improved therapeutic outcomes.
Used in Organic Synthesis:
[hydroxy(phenyl)methyl]phosphonic acid serves as a building block in the creation of various complex molecules, playing a vital role in organic synthesis. Its unique structure allows for the development of novel compounds with specific properties and applications across different industries.
Used in Medicinal and Pharmacological Research:
Due to its potential interactions with biological systems, [hydroxy(phenyl)methyl]phosphonic acid is a promising candidate for further research in the fields of medicine and pharmacology. It may lead to the discovery of new therapeutic agents or contribute to the understanding of biological processes at the molecular level.
Check Digit Verification of cas no
The CAS Registry Mumber 7252-14-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7252-14:
(6*7)+(5*2)+(4*5)+(3*2)+(2*1)+(1*4)=84
84 % 10 = 4
So 7252-14-4 is a valid CAS Registry Number.
7252-14-4Relevant articles and documents
Acylphosphonic acids and methyl hydrogen acylphosphonates: Physical and chemical properties and theoretical calculations
Karaman, Rafik,Goldblum, Amiram,Breuer, Eli,Leader, Haim
, p. 765 - 774 (2007/10/02)
Acylphosphonic acids (5) and methyl hydrogen acylphosphonates (3) were synthesized by di- and mono-demethylation of dimethyl acylphosphonates (1). Spectroscopic data (i.r., 31P and 1H n.m.r.) are reported for these types of compounds for the first time. Examination of their hydrolytic stability under acidic and basic conditions revealed that except for methyl hydrogen acylphosphonates (3) that are unstable under highly alkaline pH conditions, the C-P bond in these types of compounds is stable in most cases. Nucleophilic reagents, e.g. amines, borohydride, or hydroxylamine react with the carbonyl group of ionized acylphosphonates with the preservation of the C-P bond, to yield α-imino-, α-hydroxy-, or α-oxyimino- alkylphosphononate anions, respectively. Semi-empirical quantum mechanical (MNDO/H) calculations were performed on benzoylphosphonic acid (5c) and on the esters and anions derived from it, as representatives of their classes, in order to assess bond lengths and preferred conformations, and to estimate charges on the carbonyl and phosphoryl groups. Calculations show that for both neutral and ionized (anions) compounds free rotation around the C-P bond is expected due to the low energy barriers.
