53104-46-4 Usage
Uses
Used in Flame Retardant Industry:
(2-Hydroxyphenyl)phosphonic acid is used as a flame retardant for enhancing the fire resistance of various materials, providing safety and protection against fire hazards.
Used as a Metal Chelating Agent:
In the chemical industry, (2-Hydroxyphenyl)phosphonic acid serves as a metal chelating agent, which helps in the removal or stabilization of metal ions, improving the efficiency and performance of various processes.
Used as a Corrosion Inhibitor:
(2-Hydroxyphenyl)phosphonic acid is utilized as a corrosion inhibitor in industrial applications, preventing the degradation of metals and extending the lifespan of equipment and structures.
Used in Polymer and Plastics Production:
In the manufacturing of polymers and plastics, (2-Hydroxyphenyl)phosphonic acid plays a crucial role, contributing to the development of new materials with improved properties.
Used in Pharmaceutical Research:
(2-Hydroxyphenyl)phosphonic acid has been studied for its potential pharmaceutical applications, particularly as a potential treatment for osteoporosis and other bone-related conditions, offering new avenues for medical advancements.
Check Digit Verification of cas no
The CAS Registry Mumber 53104-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,0 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53104-46:
(7*5)+(6*3)+(5*1)+(4*0)+(3*4)+(2*4)+(1*6)=84
84 % 10 = 4
So 53104-46-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H7O4P/c7-5-3-1-2-4-6(5)11(8,9)10/h1-4,7H,(H2,8,9,10)
53104-46-4Relevant academic research and scientific papers
Phosphoryl Analogs of Salicylic Acid: Synthesis and Analgesic and Anti-Inflammatory Activity
Baulin,Kalashnikova,Vikharev, Yu. B.,Vikhareva,Baulin,Tsivadze, A. Yu.
, p. 1786 - 1791 (2018/11/24)
The synthetically convenient method of preparation of unexplored phosphoryl analogs of salicylic acid (2-hydroxyphenylphosphonic and 2-hydroxyphenylphosphinic acids) has been developed for the search of novel nonsteroidal anti-inflammatory drugs. It has been shown that 2-hydroxyphenylphosphinic acid is a lowtoxic compound (LD50 3500 mg/kg) exhibiting analgesic activity significantly higher than both 2-hydroxyphenylphosphonic acid and the reference compound (sodium metamizole).
REARRANGEMENT OF DI-T-BUTYL ARYL PHOSPHATES TO DI-T-BUTYL(2-HYDROXYARYL)PHOSPHONATES. PREPARATION OF (2-HYDROXY-1,3-PHENYLENE)BISPHOSPHONIC ACIDS
Dhavan, Balram,Redmore, Derek
, p. 177 - 182 (2007/10/02)
Di-t-butyl aryl phosphates 3 on treatment with lithium diisopropylamide rearrange to di-t-butyl (2-hydroxyaryl)phosphonates 5.A di-t-butyl (2-hydroxyaryl) phosphonate on reaction with di-t-butyl phosphorochloridate yields a phosphate-phosphonate 8 which o
o-Hydroxyaryl Diphosphonic Acids
Dhawan, Balram,Redmore, Derek
, p. 4018 - 4021 (2007/10/02)
Treatment of dialkyl aryl phosphates with n-butyllithium or lithium diisopropylamide results in a rearrangement that involves the fission of an oxygen-phosphorus bond and formation of a C-P bond yielding dialkyl (2-hydroxyaryl)phosphonates.A dialkyl (2-hy
