20753-53-1 Usage
Uses
Used in Organic Synthesis:
4-Chlorobenzeneseleninic acid is utilized as a reagent in organic synthesis for various chemical transformations. It is particularly effective in the oxidation of alcohols, where it serves as a selective and efficient oxidizing agent, converting primary and secondary alcohols into their corresponding aldehydes, ketones, or carboxylic acids.
Used in Synthesis of Selenides:
4-CHLOROBENZENESELENINIC ACID is also employed in the synthesis of selenides, which are important in the development of new materials and pharmaceuticals. The reactivity of 4-chlorobenzeneseleninic acid allows for the formation of various selenide derivatives, expanding the scope of synthetic applications.
Used in Pharmaceutical Applications:
4-Chlorobenzeneseleninic acid is a potential candidate for pharmaceutical applications due to its antioxidant and antiviral properties. Its antioxidant activity can help protect cells from oxidative stress and damage, while its antiviral properties may contribute to the development of new antiviral drugs.
However, it is crucial to consider the toxic nature of 4-chlorobenzeneseleninic acid and its potential to cause skin and eye irritation upon contact. Proper safety measures should be taken during its handling and use, and its environmental impact should be assessed when disposing of this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 20753-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,5 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20753-53:
(7*2)+(6*0)+(5*7)+(4*5)+(3*3)+(2*5)+(1*3)=91
91 % 10 = 1
So 20753-53-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H5ClO2Se/c7-5-1-3-6(4-2-5)10(8)9/h1-4H,(H,8,9)
20753-53-1Relevant academic research and scientific papers
Arylseleninic acid as a green, bench-stable selenylating agent: Synthesis of selanylanilines and 3-selanylindoles
Abenante, Laura,Anghinoni, Jo?o M.,Lenard?o, Eder J.,Padilha, Nathalia B.,Penteado, Filipe,Rosati, Ornelio,Santi, Claudio,Silva, Marcio S.
supporting information, p. 5210 - 5217 (2020/07/23)
Arylseleninic acids were used as an electrophilic selenium source in aromatic substitution reactions, using N,N-substituted anilines and indoles as nucleophiles at 70 °C for 6-15 h. A total of fourteen 4-selanylanilines and five 3-selanylindoles were selectively obtained in good to excellent yields. The starting benzeneseleninic acids are easily prepared from the respective diselenides, are bench stable and easy to handle, affording water as the only waste at the end of the reaction. This journal is
