2589-39-1 Usage
Type
Synthetic organic compound
Derivation
Derived from anthraquinone
Color
Red
Industrial Use
a. Textile industry as a dye
b. Biological research as a histological stain
Potential Applications
a. Antitumor properties
b. Antiviral properties
c. Inhibition of calcium oxalate crystal formation (kidney stones)
Traditional Medicine
Used in traditional Chinese medicine for its purported anti-inflammatory and analgesic effects
Importance
Significant compound in both industrial and scientific fields due to its wide range of potential applications
Check Digit Verification of cas no
The CAS Registry Mumber 2589-39-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2589-39:
(6*2)+(5*5)+(4*8)+(3*9)+(2*3)+(1*9)=111
111 % 10 = 1
So 2589-39-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H10O4/c1-7-6-10(16)11-12(13(7)17)15(19)9-5-3-2-4-8(9)14(11)18/h2-6,16-17H,1H3
2589-39-1Relevant academic research and scientific papers
CONDUCTING REDOX OLIGOMERS
-
Page/Page column 27, (2020/08/22)
The present disclosure relates to compounds of formula IVa or IVb, or salts thereof, as intermediates in the manufacture of conducting redox polymers. L is a covalent linker moiety and R is a reversible redox group. The disclosure further relates to conducting redox polymers produced from such compounds, as well as substrates coated with such conducting redox polymers, and organic batteries comprising such conducting redox polymers. Formule (I)
First TDAE approach in quinonic series: synthesis of new 2-substituted 1,4-dimethoxy-9,10-anthraquinones
Khoumeri, Omar,Montana, Marc,Terme, Thierry,Vanelle, Patrice
scheme or table, p. 11237 - 11242 (2009/04/11)
We report herein an original preparation of 2-substituted 1,4-dimethoxy-9,10-anthraquinones using the first example of TDAE strategy in quinonic series. This TDAE approach is an original and mild method to generate a quinonic anion, which cannot be formed via organometallic strategy.
