85392-26-3 Usage
Uses
Used in Cosmetic and Personal Care Industry:
(3-chlorophenyl)methyl 4-hydroxybenzoate is used as a preservative in the cosmetic and personal care industry to prevent the growth of microorganisms and extend the shelf-life of products. Its antimicrobial properties help maintain product integrity and safety, ensuring a longer-lasting and more effective final product for consumers.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, (3-chlorophenyl)methyl 4-hydroxybenzoate is utilized for its antimicrobial capabilities. It can be incorporated into formulations to prevent contamination and maintain the sterility of medications, ensuring their efficacy and safety for patients.
Used in Agricultural Applications:
(3-chlorophenyl)methyl 4-hydroxybenzoate also finds use in the agricultural sector, where its antimicrobial properties can be harnessed to protect crops from disease and pests. By inhibiting the growth of harmful microorganisms, (3-chlorophenyl)methyl 4-hydroxybenzoate can contribute to increased crop yields and improved food safety.
Check Digit Verification of cas no
The CAS Registry Mumber 85392-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,9 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85392-26:
(7*8)+(6*5)+(5*3)+(4*9)+(3*2)+(2*2)+(1*6)=153
153 % 10 = 3
So 85392-26-3 is a valid CAS Registry Number.
InChI:InChI=1/C14H11ClO3/c15-12-3-1-2-10(8-12)9-18-14(17)11-4-6-13(16)7-5-11/h1-8,16H,9H2
85392-26-3Relevant academic research and scientific papers
Sather, Aaron C.,Lee, Hong Geun,De La Rosa, Valentina Y.,Yang, Yang,Müller, Peter,Buchwald, Stephen L.
, p. 13433 - 13438 (2015)
A new biaryl monophosphine ligand (AlPhos, L1) allows for the room-temperature Pd-catalyzed fluorination of a variety of activated (hetero)aryl triflates. Furthermore, aryl triflates and bromides that are prone to give mixtures of regioisomeric aryl fluorides with Pd-catalysis can now be converted to the desired aryl fluorides with high regioselectivity. Analysis of the solid-state structures of several Pd(II) complexes, as well as density functional theory (DFT) calculations, shed light on the origin of the enhanced reactivity observed with L1.
