84017-99-2 Usage
Description
(S)-11-DiMethoxyMethyl-4-ethyl-4-hydroxy-1,12-dihydro-4H-2-oxa-6,12a-diaza-dibenzo[b,h]fluorene-3,13-dione is a complex organic compound characterized by its unique molecular structure. It features two methoxy groups, one ethyl group, and a hydroxy group, all attached to a dibenzo[b,h]fluorene backbone. Additionally, it contains an oxa-6,12a-diaza ring system and a 4H-3,13-dione functional group. This intricate arrangement of functional groups and molecular architecture suggests potential applications in various fields, such as pharmacology, organic synthesis, and material science. Further research and testing are necessary to explore its specific properties and potential uses.
Uses
Used in Pharmaceutical Applications:
(S)-11-DiMethoxyMethyl-4-ethyl-4-hydroxy-1,12-dihydro-4H-2-oxa-6,12a-diaza-dibenzo[b,h]fluorene-3,13-dione is used as a pharmaceutical compound for its potential therapeutic properties. The unique combination of functional groups and molecular architecture may allow it to interact with biological targets, such as receptors or enzymes, in ways that could lead to the development of new drugs for various diseases.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-11-DiMethoxyMethyl-4-ethyl-4-hydroxy-1,12-dihydro-4H-2-oxa-6,12a-diaza-dibenzo[b,h]fluorene-3,13-dione can be used as a building block or intermediate for the synthesis of more complex molecules. Its diverse functional groups and structural features make it a versatile starting material for the development of novel compounds with specific properties and applications.
Used in Material Science:
(S)-11-DiMethoxyMethyl-4-ethyl-4-hydroxy-1,12-dihydro-4H-2-oxa-6,12a-diaza-dibenzo[b,h]fluorene-3,13-dione may also find applications in material science due to its unique molecular structure. It could potentially be used in the development of new materials with specific properties, such as improved stability, reactivity, or selectivity, for use in various industries, including electronics, energy, and environmental protection.
Check Digit Verification of cas no
The CAS Registry Mumber 84017-99-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,0,1 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84017-99:
(7*8)+(6*4)+(5*0)+(4*1)+(3*7)+(2*9)+(1*9)=132
132 % 10 = 2
So 84017-99-2 is a valid CAS Registry Number.
84017-99-2Relevant articles and documents
E-ring-modified 7-oxyiminomethyl camptothecins: Synthesis and preliminary in vitro and in vivo biological evaluation
Giannini, Giuseppe,Marzi, Mauro,Cabri, Walter,Marastoni, Elena,Battistuzzi, Gianfranco,Vesci, Loredana,Pisano, Claudio,Beretta, Giovanni Luca,Cesare, Michelandrea De,Zunino, Franco
, p. 2910 - 2915 (2008)
In contrast to five-membered E-ring analogues, 7-oxyiminomethyl derivatives of homocamptothecins showed ability to form stable ternary complexes with DNA and topoisomerase I. The 7-oxyiminomethyl derivatives of homocamptothecins were evaluated as a racemi
CAMPTOTHECIN DERIVATIVES
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Page/Page column 68-69, (2010/12/31)
Various 14-Nitro, 14-amino, and 14-substituted amino camptothecin derivatives are useful in the treatment of cancer and other hyperproliferative diseases. Various 14-nitro camptothecin derivatives are conveniently prepared by reacting a camptothecin deriv
CAMPTOTHECINS WITH A MODIFIED LACTONE RING
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Page 16, (2010/11/30)
Compounds of formula (I) or (II) are described: where the groups are as defined in the description here below, the racemic mixtures, their individual enantiomers, their individual diastereoisomers, their mixtures, and their pharmaceutically acceptable sal
