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3,5-dimethoxy-4-hydroxyacetophenone radical is an organic compound characterized by its molecular formula C10H12O4. This radical is derived from acetophenone, a class of aromatic ketones, and features a hydroxyl group (-OH) at the 4-position, and two methoxy groups (-OCH3) at the 3 and 5 positions on the benzene ring. The presence of these functional groups endows the molecule with unique chemical properties, such as increased solubility in polar solvents due to the hydroxyl and methoxy groups. This radical can participate in various chemical reactions, including redox processes, and may be involved in the formation of more complex molecules or used as an intermediate in synthetic chemistry. Its stability and reactivity can be influenced by the electronic effects of the substituents on the benzene ring, making it a subject of interest in organic chemistry for potential applications in pharmaceuticals, dyes, and other industries.

2198-16-5

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2198-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2198-16-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,9 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2198-16:
(6*2)+(5*1)+(4*9)+(3*8)+(2*1)+(1*6)=85
85 % 10 = 5
So 2198-16-5 is a valid CAS Registry Number.

2198-16-5Downstream Products

2198-16-5Relevant academic research and scientific papers

A spectroscopic characterization of a phenolic natural mediator in the laccase biocatalytic reaction

Martorana, Andrea,Sorace, Lorenzo,Boer, Harry,Vazquez-Duhalt, Rafael,Basosi, Riccardo,Baratto, Maria Camilla

, p. 203 - 208 (2013)

Multi-frequency ESR combined with NALDI-TOF MS has been used for the characterization of 3,5-dimethoxy-4-hydroxyacetophenone radical intermediate and by-products formed during the Coriolopsis gallica laccase catalytic reaction. A stable radical species is formed and an intense and well-structured ESR spectrum was detected and fully characterized at S-, X- and W-bands. The presence of by-products generated as the result of by-reactions has been investigated and analyzed through NALDI-TOF MS, performing the experiments versus time. The superior radical stability of such phenoxy radical, due to steric hindrance in ortho to the phenol group and the great delocalization of the unpaired electron on the acetyl substituent, makes acetosyringone particularly interesting for biotechnological applications. This represents a good example for the development of new stable laccase mediator molecules.

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