56581-71-6 Usage
Uses
Used in Organic Synthesis:
(1Z)-1-(1-cyclopentylethylidene)-2-(2,4-dinitrophenyl)hydrazine is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the creation of new molecules with potential applications in various industries.
Used in Pharmaceutical Research:
(1Z)-1-(1-cyclopentylethylidene)-2-(2,4-dinitrophenyl)hydrazine is studied for its potential biological activities, including antimicrobial, antifungal, and larvicidal properties. Its diverse range of activities suggests that it could be a promising candidate for the development of new drugs and treatments in the pharmaceutical industry.
Used in Chemical Research:
(1Z)-1-(1-cyclopentylethylidene)-2-(2,4-dinitrophenyl)hydrazine's unique structure and properties make it a subject of interest in chemical research. Scientists are investigating its potential applications and functions in various chemical processes, which could lead to new discoveries and advancements in the field.
Check Digit Verification of cas no
The CAS Registry Mumber 56581-71-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,8 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56581-71:
(7*5)+(6*6)+(5*5)+(4*8)+(3*1)+(2*7)+(1*1)=146
146 % 10 = 6
So 56581-71-6 is a valid CAS Registry Number.
56581-71-6Relevant academic research and scientific papers
Oligomeric iodosylbenzene sulfate: A convenient hypervalent iodine reagent for oxidation of organic sulfides and alkenes
Yusubov, Mehman S.,Yusubova, Rosa Y.,Funk, Tatyana V.,Chi, Ki-Whan,Zhdankin, Viktor V.
experimental part, p. 2505 - 2508 (2009/12/08)
Oligomeric iodosylbenzene sulfate, (PhIO)3·SO 3, which can be formally considered as a partially depolymerized activated iodosylbenzene, is a readily available, stable, and water-soluble hypervalent iodine reagent that is useful for the oxidation of sulfides or alkenes. Furthermore, this reagent can be conveniently generated in situ from (diacetoxyiodo)benzene and sodium bisulfate and used without isolation in oxidations in aqueous solution or under solvent-free conditions. The reaction of iodosylbenzene sulfate in situ with organic sulfides at room temperature affords sulfoxides in high yields without over-oxidation to sulfones, and this reaction is compatible with the presence in the substrate molecule of hydroxy groups, double bonds, benzylic carbon atoms, carboxylate groups, and various substituted phenyl rings. The reaction of an alkene with iodosylbenzene sulfate generated in situ results in oxidative rearrangement to form a ketone or aldehyde. Georg Thieme Verlag Stuttgart.
