28012-58-0 Usage
Uses
Used in Pharmaceutical Applications:
1-(4-bromophenyl)-2-[(4-chlorophenyl)amino]ethanone is used as a chemical intermediate for the development of new drugs, leveraging its unique structure and properties to create novel pharmaceutical compounds.
Used in Research Applications:
In the research industry, 1-(4-bromophenyl)-2-[(4-chlorophenyl)amino]ethanone serves as a valuable compound for studying its properties and potential reactions, contributing to the advancement of chemical knowledge and the discovery of new applications.
Used in Medicinal Chemistry:
1-(4-bromophenyl)-2-[(4-chlorophenyl)amino]ethanone is used as a key component in the design and synthesis of new medicinal compounds, potentially leading to the creation of innovative treatments for various diseases and conditions.
Used in Organic Synthesis:
1-(4-bromophenyl)-2-[(4-chlorophenyl)amino]ethanone is also utilized in organic synthesis as a building block for constructing more complex molecules, which can be applied across various industries, including pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 28012-58-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,1 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28012-58:
(7*2)+(6*8)+(5*0)+(4*1)+(3*2)+(2*5)+(1*8)=90
90 % 10 = 0
So 28012-58-0 is a valid CAS Registry Number.
28012-58-0Relevant academic research and scientific papers
Ramagiri, Raj Kumar,Thupurani, Murali Krishna,Vedula, Rajeswar Rao
, p. 1713 - 1717 (2015)
A simple and highly efficient one-pot, three-component synthesis of novel substituted imidazole derivatives has been reported by the reaction of 3-(2-bromoacetyl)-2H-chromen-2-one, ammonium thiocyanate, and phenacyl aniline in the presence of acetic acid
Research on antibacterial and antifungal agents. VIII. Synthesis and antimicrobial activity of 1,4-diarylpyrroles
Porretta,Biava,Fioravanti,Fischetti,Melino,Venza,Bolle,Tita
, p. 717 - 722 (2007/10/02)
The synthesis and the antimicrobial activity of 1,4-diarylpyrroles are reported. The obtained data in comparison with pyrrolnitrin show that many acid derivatives 4 exhibit a selective activity against some strains of Candida spp and poor activity against
