139259-95-3 Usage
Uses
Used in Pharmaceutical Industry:
Acetic acid, benzoyl([1,1'-biphenyl]-4-ylmethoxy)azanyl ester is used as a key ingredient in the formulation of pharmaceuticals for its antimicrobial properties. It helps in the development of medications that combat various infections and improve overall health.
Used in Polymer and Resin Synthesis:
In the polymer and resin industry, acetic acid, benzoyl([1,1'-biphenyl]-4-ylmethoxy)azanyl ester serves as a cross-linking agent and stabilizer. It enhances the properties of polymers and resins, contributing to their durability, strength, and resistance to environmental factors.
Used in Adhesives, Coatings, and Sealants Production:
Acetic acid, benzoyl([1,1'-biphenyl]-4-ylmethoxy)azanyl ester is utilized in the production of high-performance adhesives, coatings, and sealants. Its presence in these materials improves their bonding strength, durability, and resistance to various conditions, making them suitable for a wide range of applications.
Used in Personal Care Products:
Due to its antimicrobial properties, acetic acid, benzoyl([1,1'-biphenyl]-4-ylmethoxy)azanyl ester is also used as an ingredient in personal care products. It helps maintain hygiene and prevent the growth of harmful microorganisms, ensuring the safety and effectiveness of these products.
However, it is crucial to handle acetic acid, benzoyl([1,1'-biphenyl]-4-ylmethoxy)azanyl ester with care, as it can be harmful if ingested, inhaled, or absorbed through the skin. Proper safety measures should be taken during its production, use, and disposal to minimize potential risks.
Check Digit Verification of cas no
The CAS Registry Mumber 139259-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,2,5 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 139259-95:
(8*1)+(7*3)+(6*9)+(5*2)+(4*5)+(3*9)+(2*9)+(1*5)=163
163 % 10 = 3
So 139259-95-3 is a valid CAS Registry Number.
139259-95-3Relevant academic research and scientific papers
Evidence for the Formation of Nitrenium Ions in the Acid-catalysed Solvolysis of Mutagenic N-Acetoxy-N-Alkoxybenzamides
Campbell, John J.,Glover, Stephen A.,Hammond, Gerard P.,Rowbottom, Colleen A.
, p. 2067 - 2080 (2007/10/02)
In aqueous acetonitrile, N-acetoxy-N-alkoxybenzamides undergo acid-catalysed solvolysis by the AAl1 mechanism to give acetic acid and nitrenium ions.This is indicated by an inverse dependence of the acid-independent rate constant, kH, upon the activity of water, a solvent kinetic isotope effect of 0.44 and positive Σ(excit.) values.In addition, relief of steric compression at the nitrogen enhances the rate of solvolysis.Hammett correlations with ?+ substituent constants were found for the rates of solvolysis of para-substituted-N-acetoxy-N-butoxybenzamides and N-acetoxy-N-(para-substituted benzyloxy) benzamides.This fact and the low ρ-values of -1.35 and -1.56, respectively, are indicative of a strong build-up of positive charge in the transition state which has both nitrenium ion and oxonium ion character and is in accordance with computed molecular-orbital properties of N-alkoxynitrenium ions.Greater levels of mutagenicity have been measured for those compounds which are more readily solvolysed to nitrenium ions.
