6147-43-9 Usage
Uses
Used in Organic Synthesis:
1-(2,4-dinitrophenyl)-2-(6-methylhept-5-en-2-ylidene)hydrazine is used as a reagent for various chemical reactions in the field of organic synthesis, such as condensation, reduction, and oxidation. Its unique structure allows for a wide range of applications in creating new compounds and molecules.
Used in Analytical Chemistry:
In the analysis of aldehydes and ketones, 1-(2,4-dinitrophenyl)-2-(6-methylhept-5-en-2-ylidene)hydrazine serves as a valuable reagent. It aids in the identification and quantification of these important organic compounds, which are prevalent in various chemical and biological processes.
Used in Pharmaceutical Research:
1-(2,4-dinitrophenyl)-2-(6-methylhept-5-en-2-ylidene)hydrazine has been studied for its potential as an antibacterial agent. Its ability to undergo different chemical reactions makes it a promising candidate for the development of new antibiotics to combat drug-resistant bacteria.
Used in Environmental Monitoring:
Due to the presence of the dinitrophenyl group, which poses risks of toxicity and potential environmental hazards, 1-(2,4-dinitrophenyl)-2-(6-methylhept-5-en-2-ylidene)hydrazine can be employed in environmental monitoring to detect and quantify the presence of toxic compounds in various ecosystems.
Check Digit Verification of cas no
The CAS Registry Mumber 6147-43-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,4 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6147-43:
(6*6)+(5*1)+(4*4)+(3*7)+(2*4)+(1*3)=89
89 % 10 = 9
So 6147-43-9 is a valid CAS Registry Number.
6147-43-9Relevant academic research and scientific papers
Oxidative Dehomologation of Aldehydes with Oxygen as a Terminal Oxidant
Shipilovskikh, Sergei A.,Rubtsov, Aleksandr E.,Malkov, Andrei V.
supporting information, p. 6760 - 6762 (2017/12/26)
A mild, efficient protocol for oxidative cleavage of C-C bonds in aldehydes has been developed that employs alkali metal hydrides as reagents and oxygen from air as a terminal oxidant. The method is applicable to a broad substrate range.
