55044-52-5 Usage
Uses
Used in Pharmaceutical and Chemical Industries:
[4-(methoxycarbonyl)phenyl]methyl p-toluate is used as a stabilizer and intermediate in the synthesis of organic compounds, contributing to the development of new pharmaceuticals and chemicals. Its stabilizing properties ensure the integrity and effectiveness of these compounds during production and use.
Used in Fragrance and Flavoring Production:
This chemical compound is also utilized in the creation of fragrances and flavorings, enhancing the sensory experience of various products. Its role in this industry highlights its versatility and the broad range of applications it can support.
Used in Antifungal and Antibacterial Applications:
[4-(methoxycarbonyl)phenyl]methyl p-toluate has been studied for its potential antifungal and antibacterial properties, making it a promising candidate for use in various applications where these characteristics are beneficial. Its ability to combat fungi and bacteria could lead to its incorporation in products designed to maintain cleanliness and prevent the spread of infections.
Check Digit Verification of cas no
The CAS Registry Mumber 55044-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,4 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55044-52:
(7*5)+(6*5)+(5*0)+(4*4)+(3*4)+(2*5)+(1*2)=105
105 % 10 = 5
So 55044-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H16O4/c1-12-3-7-15(8-4-12)17(19)21-11-13-5-9-14(10-6-13)16(18)20-2/h3-10H,11H2,1-2H3
55044-52-5Relevant academic research and scientific papers
Organocatalyzed anodic oxidation of aldehydes
Finney, Eric E.,Ogawa, Kelli A.,Boydston, Andrew J.
supporting information; experimental part, p. 12374 - 12377 (2012/09/05)
A method for the catalytic formation of electroauxiliaries and subsequent anodic oxidation has been developed. The process interfaces N-heterocyclic carbene-based organocatalysis with electro-organic synthesis to achieve direct oxidation of catalytically generated electroactive intermediates. We demonstrate the applicability of this method as a one-pot conversion of aldehydes to esters for a broad range of aldehyde and alcohol substrates. Furthermore, the anodic oxidation reactions are very clean, producing only H2 gas as a result of cathodic reduction.
