2675-29-8 Usage
Uses
Used in Pharmaceutical Industry:
Ethanone, 1-(4-aminophenyl)-, (4-nitrophenyl)hydrazone is used as a reagent for the detection and measurement of aldehydes and ketones. Its ability to react with carbonyl compounds to form brightly colored derivatives makes it a valuable tool in the pharmaceutical industry for visualizing and quantifying these functional groups.
Used in Analytical Chemistry:
In analytical chemistry, Ethanone, 1-(4-aminophenyl)-, (4-nitrophenyl)hydrazone is employed as a reagent for the detection and measurement of aldehydes and ketones. Its reaction with carbonyl compounds to form brightly colored derivatives allows for the visualization and quantification of these functional groups, making it a crucial component in various scientific processes.
Used in Antibacterial and Antifungal Applications:
Ethanone, 1-(4-aminophenyl)-, (4-nitrophenyl)hydrazone has been studied for its potential antibacterial and antifungal properties. Its ability to inhibit the growth of certain bacteria and fungi suggests that it could be used in the development of new therapeutic agents, particularly in the fields of medicine and healthcare.
Overall, Ethanone, 1-(4-aminophenyl)-, (4-nitrophenyl)hydrazone plays a significant role in various scientific and industrial processes due to its reactive and versatile nature. Its applications in the pharmaceutical industry, analytical chemistry, and potential use in the development of new therapeutic agents highlight its importance in the scientific community.
Check Digit Verification of cas no
The CAS Registry Mumber 2675-29-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,7 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2675-29:
(6*2)+(5*6)+(4*7)+(3*5)+(2*2)+(1*9)=98
98 % 10 = 8
So 2675-29-8 is a valid CAS Registry Number.
2675-29-8Relevant academic research and scientific papers
AlCl3·6H2O-catalyzed Schiff-base reaction between aryl ketones and aromatic acylhydrazines/hydrazines in water
Zhao, Zhi Xiang,Li, Ting,Cheng, Li Ping,Li, Meng,Zhong, Zhi Jian,Pang, Wan
, p. 1833 - 1839 (2019/11/05)
Abstract: Schiff-bases have important applications in the field of analysis, biomedicine, as well as material sciences. Hydrazones and acylhydrazones are two representative types of Schiff-bases. In this study, a green synthesis of aromatic hydrazones and
