1093-62-5 Usage
Description
(2-phenoxyphenyl)phenylphosphinic acid is an organophosphorus compound with the chemical formula C18H15O3P. It is recognized for its unique chemical structure and properties, which make it a versatile precursor in the synthesis of phosphine oxides. These phosphine oxides are valuable in catalysis and coordination chemistry as ligands. Furthermore, this compound has demonstrated insecticidal properties, positioning it as a potential candidate for use in pesticides. Its exploration also extends to the development of flame retardants and polymer additives, capitalizing on its distinctive characteristics.
Uses
Used in Chemical Synthesis Industry:
(2-phenoxyphenyl)phenylphosphinic acid is used as a precursor for the synthesis of phosphine oxides, which are essential in the development of catalysts and as ligands in coordination chemistry. Its role in this industry is pivotal for creating compounds that facilitate various chemical reactions and contribute to the advancement of material sciences.
Used in Pesticide Development:
Due to its insecticidal properties, (2-phenoxyphenyl)phenylphosphinic acid is being studied for its potential use as a pesticide. It offers a promising avenue for the development of new and effective pest control solutions in agriculture and related fields, aiming to enhance crop protection and yield.
Used in Flame Retardant Production:
(2-phenoxyphenyl)phenylphosphinic acid is being investigated for its potential application in the production of flame retardants. Its unique chemical structure and properties make it a candidate for creating safer and more effective flame retardants, which are crucial for preventing fires and ensuring safety in various industries.
Used in Polymer Additives Industry:
(2-phenoxyphenyl)phenylphosphinic acid is also being explored for its use in the development of polymer additives. Its incorporation into polymers can enhance their performance, providing benefits such as improved stability, durability, and resistance to environmental factors. This application is vital for the plastics and materials industry, where innovation in additives can lead to the creation of new and improved products.
Check Digit Verification of cas no
The CAS Registry Mumber 1093-62-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,9 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1093-62:
(6*1)+(5*0)+(4*9)+(3*3)+(2*6)+(1*2)=65
65 % 10 = 5
So 1093-62-5 is a valid CAS Registry Number.
1093-62-5Relevant articles and documents
Experimental and quantum chemical studies of 2-phosphinylphenol derivatives
Levy, Jack B.,Sutton, Steven B.,Olsen, Ronald E.
, p. 601 - 604 (2007/10/03)
Carbon-oxygen bonds ortho to a phosphoryl group in triarylphosphine oxides undergo cleavage when the oxides are either fused with potassium hydroxide or treated with potassium tert-butoxide in refluxing toluene, presumably through a nucleophilic addition-elimination mechanism. Thus, bis(2-hydroxyphenyl)phenylphosphine oxide is produced along with the expected 2-phenoxyphenyl(phenyl)phosphinic acid from 10-phenyl-10H-phenoxaphosphine 10-oxide. The latter starting material is also produced, together with bis(2-hydroxyphenyl)phenylphosphine oxide, when bis(2-methoxyphenyl)phenylphosphine oxide is fused with potassium hydroxide. Fusion of bis(2-methoxyphenyl)phenylphosphine oxide with sodium hydroxide, however, yields 2-hydroxyphenyl(phenyl)phosphinic acid. Ab initio quantum chemical studies confirm that the downfield 31P chemical shift that is observed in 2-phosphinylphenols is due to hydrogen bonding to the phosphoryl group.
