66248-82-6 Usage
Uses
Used in Pharmaceutical Industry:
Ethanone, 1-(4-methoxy-2-methylphenyl)-2-phenylis used as a precursor in the synthesis of various drugs for its potential medicinal properties. Its chemical structure allows for the development of new pharmaceutical compounds that can address specific medical needs.
Used in Fragrance and Flavoring Industry:
Ethanone, 1-(4-methoxy-2-methylphenyl)-2-phenylis used as a key ingredient in the production of fragrances and flavorings due to its aromatic properties. Its unique scent and flavor characteristics contribute to the creation of diverse and appealing products in these industries.
Further research is needed to fully understand the biological activities and potential applications of Ethanone, 1-(4-methoxy-2-methylphenyl)-2-phenylin various industries, including its possible use in other areas such as cosmetics, food additives, or as a research tool in scientific studies.
Check Digit Verification of cas no
The CAS Registry Mumber 66248-82-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,4 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66248-82:
(7*6)+(6*6)+(5*2)+(4*4)+(3*8)+(2*8)+(1*2)=146
146 % 10 = 6
So 66248-82-6 is a valid CAS Registry Number.
66248-82-6Relevant academic research and scientific papers
Veeramaneni, Venugopal Rao,Pal, Manojit,Yeleswarapu, Koteswar Rao
, p. 3283 - 3290 (2003)
In this report, we describe the parallel as well as conventional synthesis of 1,2-diaryl-1-ethanones via environmentally benign acylation of arenes with in situ generated arylacetyl trifluoroacetates. A wide variety of arylacetic acids I participated in trifluoroacetic anhydride/phosphoric acid mediated C-C bond formation reaction when reacted with arenes of type II to give 1,2-diaryl-1-ethanones III in good to excellent yield. Under the solvent-free conditions these chemical transformations that normally require longer reaction time can be performed within minutes in good yield.
