57998-68-2 Usage
Uses
Used in Antineoplastic Applications:
DIAZIQUONE is utilized as an antineoplastic agent, which means it is employed in the treatment and management of neoplastic (cancerous) conditions. Its unique chemical structure allows it to interfere with essential cellular processes in cancer cells, thereby inhibiting their growth and proliferation. This makes DIAZIQUONE a valuable compound in the fight against cancer.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, DIAZIQUONE is used as a key component in the development of novel therapeutic agents targeting cancer. Its specific chemical properties and antineoplastic activity make it a promising candidate for the creation of innovative drugs and treatment strategies aimed at improving patient outcomes and overcoming resistance to existing cancer therapies.
Used in Research and Development:
DIAZIQUONE also plays a significant role in research and development, particularly in the field of cancer biology and drug discovery. Its unique structure and biological activity make it an interesting subject for further investigation, potentially leading to the discovery of new mechanisms of action and the development of more effective cancer treatments.
Safety Profile
Poison by intravenous andintraperitoneal routes. Human mutation data reported.When heated to decomposition it emits toxic fumes ofNOx.
Check Digit Verification of cas no
The CAS Registry Mumber 57998-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,9 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57998-68:
(7*5)+(6*7)+(5*9)+(4*9)+(3*8)+(2*6)+(1*8)=202
202 % 10 = 2
So 57998-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H20N4O6/c1-3-25-15(23)17-9-11(19-5-6-19)14(22)10(18-16(24)26-4-2)12(13(9)21)20-7-8-20/h3-8H2,1-2H3,(H,17,23)(H,18,24)
57998-68-2Relevant academic research and scientific papers
1,4-Benzoquinones: Improved Methods of Synthesis and New Diaziridinyl Analogues
Dzielendziak, Adam,Butler, John
, p. 643 - 645 (2007/10/02)
Two methods are given for the synthesis of 2,5-dichloro-3,6-bis(alkoxycarbonylamino)-1,4-benzoquinones 4, which can be subsequently reacted with aziridine to produce novel 2,5-di(1-aziridinyl)-3,6-bis(alkoxycarbonylamino)-1,4-benzoquinones 5.The first met
Method for producing 3,6-bis(carboethoxyamino)-2,5-diaziridinyl-1,4-benzoquinone
-
, (2008/06/13)
A method is described of preparing a diaziridinyl diaminobenzoquinone-N, N'-dicarboxylate compound selected from dialkyl, di(arylalkyl), or diphenyl diaminobenzoquinone-N, N'-dicarboxylates, said method comprising: reacting a diaminohydroquinone of the formula: STR1 wherein X is selected from the group consisting of chlorine, fluorine, bromine, iodine or alkoxy groups with a molar excess of a pyrocarbonate di-substituted with alkyl groups, arylalkyl groups, or phenyl groups to produce a dialkyl, a di(arylalkyl), or a diphenyl diaminohydroquinone-N,N'-dicarboxylate; oxidizing said hydroquinone to the respective benzoquinone; reacting said benzonquinone with an aziridine having no substitution on the nitrogen and having substituents on the carbons selected from the group consisting of hydrogen and alkyl; and recovering the resultant diazirindinyl diaminobenzoquinone-N,N'-dicarboxylate.
