113361-73-2 Usage
Uses
Used in Fragrance Industry:
1-(4-ethoxy-3,5-dimethylphenyl)ethanone is used as a fragrance ingredient for its sweet, floral odor, making it a valuable component in the creation of perfumes and personal care products. Its unique scent profile contributes to the overall aroma of these products, enhancing the sensory experience for consumers.
Used in Organic Synthesis:
In the field of organic chemistry, 1-(4-ethoxy-3,5-dimethylphenyl)ethanone serves as a building block and reagent in the preparation of other organic compounds. Its versatile structure allows for further modification and functionalization, making it a useful starting material for the synthesis of a wide range of chemical products.
Used in Pharmaceutical Industry:
Due to its unique chemical properties, 1-(4-ethoxy-3,5-dimethylphenyl)ethanone has potential applications in the pharmaceutical industry. It may be utilized in the development of new drugs or as an intermediate in the synthesis of existing medications, contributing to the advancement of medical treatments.
Used in Agrochemical Industry:
Similarly, the compound's distinctive characteristics make it a candidate for use in the agrochemical industry. It may be employed in the development of new pesticides, herbicides, or other agricultural chemicals, helping to improve crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 113361-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,6 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113361-73:
(8*1)+(7*1)+(6*3)+(5*3)+(4*6)+(3*1)+(2*7)+(1*3)=92
92 % 10 = 2
So 113361-73-2 is a valid CAS Registry Number.
113361-73-2Relevant academic research and scientific papers
Synthesis and preliminary pharmacological evaluation of aryl dithiolethiones with cyclooxygenase-2-selective inhibitory activity and hydrogen sulfide-releasing properties
Zanatta, Shannon D.,Jarrott, Bevyn,Williams, Spencer J.
scheme or table, p. 946 - 957 (2011/08/05)
A series of 5-aryl-1,2-dithiolethiones and 5-aryl-1,2-dithiole-3-ones were investigated as hydrogen sulfide-releasing anti-inflammatory drugs. Generally, phenolic acetophenones were best protected by methoxymethyl groups and the dithiolethione group insta
DITHIOLE COMPOUNDS AS COX INHIBITORS
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Page/Page column 40, (2008/12/05)
A compound of formula (I) wherein: R1 and R2 are the same or different and are independently selected from H and a shielding group; X and Y are each independently selected from N and CH; R3 is hydroxy, alkoxy, acyloxy or a
