5327-72-0 Usage
Uses
Used in Organic Synthesis:
1,4-diaminoanthracene-9,10-diol is utilized as a building block in organic synthesis for various chemical reactions, providing a foundation for the creation of new compounds and materials.
Used in Dye and Pigment Production:
As a precursor, 1,4-diaminoanthracene-9,10-diol is employed in the production of dyes and pigments, leveraging its chemical structure to contribute to the color and properties of these products.
Used in Medical Research:
1,4-diaminoanthracene-9,10-diol has potential applications in the field of medicine, particularly in cancer research. It is studied for its ability to interact with DNA, which may lead to the inhibition of cancer cell growth, offering a new avenue for therapeutic development.
However, it is important to note that 1,4-diaminoanthracene-9,10-diol, like many chemical compounds, poses potential health risks. Therefore, it should be handled with caution in laboratory and industrial settings to ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 5327-72-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5327-72:
(6*5)+(5*3)+(4*2)+(3*7)+(2*7)+(1*2)=90
90 % 10 = 0
So 5327-72-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N2O2/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-6,17-18H,15-16H2
5327-72-0Relevant articles and documents
Synthesis and antiproliferative activity of 1,4-bis(dimethylamino)-9,10- anthraquinone derivatives against P388 mouse leukemic tumor cells
Jin, Guang-Zhu,Jin, Hai-Shan,Jin, Li-Li
experimental part, p. 1071 - 1076 (2012/07/27)
A series of 2-substituted-1,4-bis(dimethylamino)-9,10-anthraquinone derivatives were synthesized and their in vitro antiproliferative activities against p388 mouse leukemic tumor cells were evaluated. In addition, the effect of substituents on the phenyl ring was investigated. Among the derivatives tested, seven showed a high antiproliferative effect and three showed a moderate effect. In addition, introduction of a series of substituted phenyl groups into 1,4-bis(dimethylamino)-9,10-anthraquinone at 2-position were shown to enhance its antiproliferative activity. The antiproliferative activity also increased upon substitution of the benzene ring by an electron donating group such as an amine or methoxyl group.
