168129-73-5 Usage
Uses
Used in Agricultural Products:
Phosphonic acid, [phenyl(phenylseleno)methyl]-, diethyl ester is used as a component in the production of agricultural products for its ability to enhance crop yield and protect plants from diseases and pests.
Used in Water Treatment:
In the water treatment industry, Phosphonic acid, [phenyl(phenylseleno)methyl]-, diethyl ester is utilized as a water treatment agent to remove impurities and contaminants, ensuring the quality and safety of water for various industrial applications.
Used in Industrial Processes:
Phosphonic acid, [phenyl(phenylseleno)methyl]-, diethyl ester is employed as a component in various industrial processes due to its unique chemical structure and reactivity, contributing to the development of new materials and products.
Used in Food Preservation:
Phosphonic acid, [phenyl(phenylseleno)methyl]-, diethyl ester is used as a preservative in the food industry to extend the shelf life of products and prevent spoilage, thanks to its strong antimicrobial properties.
Used in Pharmaceutical Industry:
Due to its unique chemical properties, Phosphonic acid, [phenyl(phenylseleno)methyl]-, diethyl ester has potential applications in the pharmaceutical industry, where it can be used in the development of new drugs and therapies.
However, it is crucial to handle Phosphonic acid, [phenyl(phenylseleno)methyl]-, diethyl ester with care, as it may have potential toxicity and environmental impact. Proper safety measures and regulations should be followed to minimize any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 168129-73-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,1,2 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 168129-73:
(8*1)+(7*6)+(6*8)+(5*1)+(4*2)+(3*9)+(2*7)+(1*3)=155
155 % 10 = 5
So 168129-73-5 is a valid CAS Registry Number.
168129-73-5Relevant academic research and scientific papers
Studies on the Free Radical Carbon-Carbon Bond Formation in the Reaction of α-Phosphoryl Sulfides and Selenides with Alkenes
Balczewski, Piotr,Pietrzykowski, Witold M.,Mikolajczyk, Marian
, p. 7727 - 7740 (2007/10/02)
α-Mono- and α,α-disubstituted α-phosphoryl radicals 9 were generated from the easy accessible α-phosphoryl sulfides 4, 5 and α-phosphoryl selenides 11, 12 and reacted with the electron rich alkenes 6 under the reductive (n-Bu3SnH/AIBN) conditions to give the functionalized phosphonates 7 in 32+68percent yield.Two fragmentation processes of the phosphonate α-alkoxy alkyl radicals are also described. - Key words: α-phosphoryl sulfides, α-phosphoryl selenides, intermolecular radical reaction, radical fragmentation, phosphonates, tri-n-butyltin hydride, α,α'-azaisobutyronitrile
