13507-52-3 Usage
Uses
Used in Chemical and Biochemical Processes:
(2-oxo-2H-chromen-3-yl)phosphonic acid is used as a chelating agent for its ability to bind metal ions effectively, which is beneficial in various chemical and biochemical processes.
Used in Industrial Applications:
In the industry, (2-oxo-2H-chromen-3-yl)phosphonic acid is used as a metal processing aid and in water treatment due to its strong metal ion binding capabilities, which help in the efficient management of metal contaminants.
Used in Pharmaceutical Research:
(2-oxo-2H-chromen-3-yl)phosphonic acid is studied for its potential as an antiviral and anticancer agent, making it a compound of interest in the field of pharmaceutical research and drug development.
Used in Metal Ion Management:
(2-oxo-2H-chromen-3-yl)phosphonic acid is utilized for managing metal ion concentrations in different industrial and environmental applications, where controlling metal ion levels is crucial for process efficiency and safety.
Check Digit Verification of cas no
The CAS Registry Mumber 13507-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,0 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13507-52:
(7*1)+(6*3)+(5*5)+(4*0)+(3*7)+(2*5)+(1*2)=83
83 % 10 = 3
So 13507-52-3 is a valid CAS Registry Number.
13507-52-3Relevant academic research and scientific papers
Reaction of 3-bromobenzyl and 3-bromoacetyl coumarin with phosphites. Synthesis of some new phosphonates and phosphates in the coumarin series
Nikolova, Rositca,Bojilova, Anka,Rodios, Nestor A.
, p. 14407 - 14420 (2007/10/03)
The reaction of 3-(1-bromobenzyl)coumarin 3 with trialkyl phosphites afforded in good yields the corresponding dialkyl phosphonates 5, the Arbuzov reaction products. The interaction of trialkyl phosphites with 3-(ω- bromoacetyl)coumarin 4 gave the corresponding dialkyl vinylphosphates 8 as the only isolated products, whereas dialkyl phosphites reacted with 4 under phase transfer catalysis and gave vinylphosphates 8 or dialkyl 1,2-epoxy- ethylphosphonates 9. The β-oxo-phosphonates 7 were obtained from the reaction of hydrazone-derivative 10 with trialkyl phosphites and the subsequent hydrolysis of the dialkyl β-hydrazono-phosphonates 11 thus formed.
