69938-73-4 Usage
Uses
Used in Pharmaceutical Applications:
Used in Antimicrobial Applications:
In the field of antimicrobial applications, [2,2':7',2''-Ternaphthalene]-1,1',1'',4,4',4''-hexone,8,8',8''-trihydroxy-6,6',6''-trimethylis used as an antimicrobial agent due to its ability to exhibit antimicrobial activities, which can be beneficial in the development of new antibiotics or antifungal agents.
Used in Histological Staining Techniques:
[2,2':7',2''-Ternaphthalene]-1,1',1'',4,4',4''-hexone,8,8',8''-trihydroxy-6,6',6''-trimethylis used as a dye in histological staining techniques, taking advantage of its orange-red color for visualizing and differentiating various cellular structures in biological samples.
Used in Chemical Research:
In the chemical research industry, [2,2':7',2''-Ternaphthalene]-1,1',1'',4,4',4''-hexone,8,8',8''-trihydroxy-6,6',6''-trimethylis used as a compound of interest for its diverse chemical and biological properties, which can lead to advancements in the understanding of polyaromatic ketone derivatives and their potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 69938-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,3 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69938-73:
(7*6)+(6*9)+(5*9)+(4*3)+(3*8)+(2*7)+(1*3)=194
194 % 10 = 4
So 69938-73-4 is a valid CAS Registry Number.
69938-73-4Relevant academic research and scientific papers
Regioselective Syntheses of 3,3'-Bijuglone, Mamegakinone, Dianellinone, cyclo-Trijuglone, Xylospyrin, and Trianellinone by Phenol-Quinone Addition
Brockmann, Hans,Laatsch, Hartmut
, p. 433 - 447 (2007/10/02)
Regioselective phenol-quinone addition of juglone (1a), 7-methyljuglone (1b), and stypandrone (1c) in pyridine yields the dimers 3,3-bijuglone (5a), mamegakinone (5c), and dianellinone (5e).In acetic acid mainly the cyclo trimers cyclo-trijuglone (12a), xylospyrin (12d), and trianellinone (12g) are obtained.
