16101-29-4 Usage
Description
1-(acetyloxy)-5-oxo-1,2,3,4,4a,5-hexahydrophenazin-5-ium, commonly known as acetylphenazin-5-ium, is a heterocyclic chemical compound featuring a phenazine ring structure. As a quaternary ammonium salt, it possesses a positively charged nitrogen atom and has been explored for its pharmaceutical potential, particularly in drug development. Additionally, it serves as a redox-active dye in biochemistry and molecular biology due to its ability to participate in redox reactions and exhibit fluorescence properties.
Uses
Used in Organic Chemistry:
1-(acetyloxy)-5-oxo-1,2,3,4,4a,5-hexahydrophenazin-5-ium is used as a reagent in the field of organic chemistry for various synthetic applications, leveraging its unique chemical structure and properties.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1-(acetyloxy)-5-oxo-1,2,3,4,4a,5-hexahydrophenazin-5-ium is used as a compound with potential pharmaceutical properties, contributing to the development of new drugs due to its redox activity and other characteristics.
Used in Biochemistry and Molecular Biology:
1-(acetyloxy)-5-oxo-1,2,3,4,4a,5-hexahydrophenazin-5-ium is utilized as a redox-active dye in studies related to biochemistry and molecular biology, where its ability to undergo redox reactions and fluorescence properties are of significant interest.
Overall, 1-(acetyloxy)-5-oxo-1,2,3,4,4a,5-hexahydrophenazin-5-ium is a versatile and significant chemical compound with a broad spectrum of potential applications across different scientific disciplines.
Check Digit Verification of cas no
The CAS Registry Mumber 16101-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,0 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16101-29:
(7*1)+(6*6)+(5*1)+(4*0)+(3*1)+(2*2)+(1*9)=64
64 % 10 = 4
So 16101-29-4 is a valid CAS Registry Number.
16101-29-4Relevant articles and documents
Unusual friedlander reactions: A route to novel quinoxaline-based heterocycles
Shoker, Tharallah A.,Ghattass, Khaled I.,Fettinger, James C.,Kurth, Mark J.,Haddadin, Makhluf J.
, p. 3704 - 3707 (2012)
Acid catalyzed Friedlander reactions of a number of 2,3-dihydro-1H- cyclopenta[b]quinoxaline-1-ones with 2-aminobenzaldehyde yield, unexpectedly, 8H-indolo[3,2-a]phenazine and quinolino[2,3-c]cyclopentadienone[2,3-b] quinoxalines, the structures of derivatives of which were confirmed by X-ray crystallography. Easy routes to novel quinoxaline-based indoles, quinolones, and quinoxaline-1,4-dioxides are reported, and proposed mechanisms for the unexpected products are discussed.
