112446-20-5 Usage
Uses
Used in Pharmaceutical and Chemical Research:
Ethanone, 1-[5-bromo-2-(phenylthio)phenyl]is used as a building block and reagent in the synthesis of organic compounds and various chemical reactions, contributing to the development of new pharmaceutical and chemical products.
Used in Drug Development:
Due to its unique structure and potential biological activity, Ethanone, 1-[5-bromo-2-(phenylthio)phenyl]is utilized in the development of pharmaceutical drugs, particularly in the areas of cancer research and antimicrobial therapy.
Used in Agrochemical Product Development:
Ethanone, 1-[5-bromo-2-(phenylthio)phenyl]is also employed in the development of agrochemical products, leveraging its reactivity and versatile properties to create new compounds for agricultural applications.
Used in Cancer Research:
Ethanone, 1-[5-bromo-2-(phenylthio)phenyl]has been studied for its potential therapeutic applications in cancer research, where its unique structure may contribute to the discovery of new cancer treatments.
Used in Antimicrobial Development:
In the field of antimicrobial development, Ethanone, 1-[5-bromo-2-(phenylthio)phenyl]is explored for its potential to contribute to the creation of new antimicrobial agents, addressing the growing need for effective treatments against resistant pathogens.
Check Digit Verification of cas no
The CAS Registry Mumber 112446-20-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,4 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112446-20:
(8*1)+(7*1)+(6*2)+(5*4)+(4*4)+(3*6)+(2*2)+(1*0)=85
85 % 10 = 5
So 112446-20-5 is a valid CAS Registry Number.
112446-20-5Relevant academic research and scientific papers
4-SUBSTITUTED 1-(1-(2-(ARYLTHIO)-5-HALOGENOPHENYL)ETHYL)PIPERAZINES; SYNTHESIS AND BIOLOGICAL SCREENING
Valenta, Vladimir,Holubek, Jiri,Protiva, Miroslav
, p. 1062 - 1072 (2007/10/02)
Reactions of 2,5-dichloroacetophenone and 2,5-dibromoacetophenone with a series of thiophenols gave the 2-(arylthio)-5-halogenoacetophenones VII and VIII which were reduced with sodium borohydride in ethanol to the secondary alcohols IX and X.Treatment wi
