15221-84-8 Usage
Description
1-(4-CHLOROPHENYL)-2-(4-METHYLPHENYL)ETHAN-1-ONE, with the molecular formula C15H13ClO, is a ketone compound featuring a chlorophenyl group and a methylphenyl group. It is widely recognized for its utility in organic synthesis and medicinal chemistry, serving as a fundamental building block for the creation of diverse pharmaceuticals and organic molecules.
Uses
Used in Pharmaceutical Industry:
1-(4-CHLOROPHENYL)-2-(4-METHYLPHENYL)ETHAN-1-ONE is used as a key intermediate for the development of new drugs, leveraging its unique chemical structure to contribute to the design and synthesis of innovative pharmaceutical compounds.
Used in Research and Development:
In the realm of research, 1-(4-CHLOROPHENYL)-2-(4-METHYLPHENYL)ETHAN-1-ONE is utilized as a starting material for the synthesis of complex organic compounds, furthering the understanding of its chemical properties and potential applications in various fields.
Used in Organic Synthesis:
1-(4-CHLOROPHENYL)-2-(4-METHYLPHENYL)ETHAN-1-ONE is also employed as a valuable building block in organic synthesis, where its chlorophenyl and methylphenyl groups can be strategically modified to produce a range of organic molecules with specific functionalities and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 15221-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,2 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15221-84:
(7*1)+(6*5)+(5*2)+(4*2)+(3*1)+(2*8)+(1*4)=78
78 % 10 = 8
So 15221-84-8 is a valid CAS Registry Number.
15221-84-8Relevant articles and documents
Thianthrenation-enabled α-arylation of carbonyl compounds with arenes
Huang, Yu-Hao,Nie, Xiao-Xue,Wang, Peng
supporting information, p. 7716 - 7720 (2020/11/02)
The Pd-catalyzed α-arylation of carbonyl compounds with simple arenes enabled by site-selective thianthrenation has been demonstrated. This onepot process using thianthrenium salts as the traceless arylating reagents features mild conditions and a broad substrate scope. In addition, this protocol could also tolerate the heterocyclic carbonyl compounds and complex bioactive molecules, which is appealing for medicinal chemistry.
