259827-72-0 Usage
Uses
Used in Pesticide Industry:
Phosphonic acid, hexyl-, methyl 4-nitrophenyl ester is used as a pesticide for its ability to inhibit the growth of microorganisms, making it an effective agent in controlling pests and diseases in agriculture.
Used in Pharmaceutical Industry:
This chemical compound is used as a component in the synthesis of pharmaceuticals, contributing to the development of various medications and treatments.
Used in Plastic and Rubber Manufacturing:
Phosphonic acid, hexyl-, methyl 4-nitrophenyl ester is used in the production of plastic and rubber materials, enhancing their properties and performance in various applications.
Used as an Antimicrobial Agent:
Due to its ability to inhibit microbial growth, phosphonic acid, hexyl-, methyl 4-nitrophenyl ester is used as an antimicrobial agent in various industries, such as in the production of medical devices and consumer products to prevent the spread of infections.
Check Digit Verification of cas no
The CAS Registry Mumber 259827-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,8,2 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 259827-72:
(8*2)+(7*5)+(6*9)+(5*8)+(4*2)+(3*7)+(2*7)+(1*2)=190
190 % 10 = 0
So 259827-72-0 is a valid CAS Registry Number.
259827-72-0Relevant academic research and scientific papers
Wikmark, Ylva,Engelmarkcassimjee, Karim,Lihammar, Richard,B?ckvall, Jan-E.
, p. 141 - 145 (2016)
A mobile region is proposed to be a flap that covers the active site of Candida antarctica lipaseA. Removal of the mobile region retains the functional properties of the enzyme. Interestingly interfacial activation, required for the wild-type enzyme, was not observed for the truncated variant, although stability, activity, and stereoselectivity were very similar for the wild-type and variant enzymes. The variant followed classical Michaelis-Menten kinetics, unlike the wild type. Both gave the same relative specificity in the transacylation of a primary and a secondary alcohol in organic solvent. Furthermore, both showed the same enantioselectivity in transacylation of alcohols and the hydrolysis of alcohol esters, as well as in the hydrolysis of esters chiral at the acid part.
