5417-20-9 Usage
Uses
Used in Pharmaceutical Research:
1-(3,4-dimethoxy-2-methylphenyl)ethanone is used as a building block for the development of new medications. Its unique chemical structure allows for the creation of a diverse range of pharmaceutical compounds, making it a valuable asset in the field of drug discovery and design.
Used in Agrochemicals:
In the agrochemical industry, 1-(3,4-dimethoxy-2-methylphenyl)ethanone is utilized as an intermediate for the synthesis of various agrochemicals. Its versatility in chemical reactions enables the production of a wide array of compounds with potential applications in agriculture, such as pesticides and herbicides.
Used in Organic Synthesis:
As a key component in organic synthesis, 1-(3,4-dimethoxy-2-methylphenyl)ethanone is employed in the preparation of a variety of organic compounds. Its unique structure and reactivity make it a valuable tool for chemists working on the synthesis of complex molecules.
Used in Antimicrobial Applications:
1-(3,4-dimethoxy-2-methylphenyl)ethanone has been studied for its potential antimicrobial properties. Researchers are exploring its use as a component in the development of new antimicrobial agents to combat drug-resistant bacteria and other pathogens.
Used in Antioxidant Applications:
Due to its antioxidant properties, 1-(3,4-dimethoxy-2-methylphenyl)ethanone is being investigated for its potential use in the development of antioxidant compounds. These compounds could be utilized in various industries, such as the food and pharmaceutical industries, to extend the shelf life of products and protect against oxidative damage.
Check Digit Verification of cas no
The CAS Registry Mumber 5417-20-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5417-20:
(6*5)+(5*4)+(4*1)+(3*7)+(2*2)+(1*0)=79
79 % 10 = 9
So 5417-20-9 is a valid CAS Registry Number.
5417-20-9Relevant academic research and scientific papers
Catechol O-methyltransferase. 12. Affinity Labeling the Active Site with the Oxidation Products of 5,6-Dihydroxyindole
Borchardt, Ronald T.,Bhatia, Pramila
, p. 263 - 271 (2007/10/02)
5,6-Dihydroxyindole (5,6-DHI) and a series of 4- and/or 7-methylated analogues of 5,6-DHI have been synthesized and evaluated for their ability to inactivate purified liver rat catechol O-methyltransferase (COMT).The inactivation of COMT by these agents could be prevented by excluding oxygen from the incubation mixtures, indicating the necessity for their oxidation to the corresponding aminochromes.Substrate protection studies and kinetic studies suggested that the loss of enzyme activity resulted from the modification of a crucial amino acid residue at the active site of COMT through reaction with the quinoid oxidation products.The COMT inhibitory activity of the 4- and/or 7-methylazed analogues of 5,6-DHI argue against a mechanism involving a 1,4 Michael addition reaction at positions 4 or 7 on the aminochrome.Cnsidering the number of potential eletrophilic centers on the basic aminochrome structure, the site of the reaction might change depending on the aromatic substitution pattern.The preferred pathway of reaction may be determined in part by the juxtaposition of the protein nucleophile to the possible sites of attack on the electrophilic ligand but also in part on the reactivity of the electrophilic site which might change with substitution on the aromatic ring.
