CAS 568-93-4
:1,2-Dihydroxy-3-nitro-9,10-anthracenedione
Description:
1,2-Dihydroxy-3-nitro-9,10-anthracenedione, also known as nitroanthraquinone, is an organic compound characterized by its anthraquinone structure, which features a fused ring system. This compound contains two hydroxyl (-OH) groups and one nitro (-NO2) group, contributing to its chemical reactivity and potential applications. It typically appears as a solid, often with a deep color due to the presence of conjugated double bonds in its structure. The hydroxyl groups can participate in hydrogen bonding, influencing its solubility and interaction with other molecules. The nitro group introduces electrophilic characteristics, making it a candidate for various chemical reactions, including nitration and reduction processes. This compound is of interest in fields such as organic synthesis, dye production, and materials science, where its properties can be exploited for specific applications. Safety considerations should be taken into account, as nitro compounds can be hazardous and may require careful handling and storage.
Formula:C14H7NO6
InChI:InChI=1S/C14H7NO6/c16-11-6-3-1-2-4-7(6)12(17)10-8(11)5-9(15(20)21)13(18)14(10)19/h1-5,18-19H
InChI key:InChIKey=XZSUEVFAMOKROK-UHFFFAOYSA-N
SMILES:O=C1C=2C(C(=O)C=3C1=CC=CC3)=CC(N(=O)=O)=C(O)C2O
Synonyms:- 1,2-Dihydroxy-3-Nitroanthracene-9,10-Dione
- 1,2-Dihydroxy-3-nitro-9,10-anthracenedione
- 1,2-Dihydroxy-3-nitro-9,10-anthraquinone
- 209-310-2
- 3-Nitroalizarin
- 3-Nitroalizarine
- 568-93-4
- 9,10-Anthracenedione, 1,2-dihydroxy-3-nitro-
- Alizarin orange
- Alizarine Orange A
- Alizarine orange
- Anthraquinone, 1,2-dihydroxy-3-nitro-
- NSC 37586
- β-Nitroalizarin
- See more synonyms
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Found 4 products.
1,2-Dihydroxy-3-nitroanthraquinone
CAS:1,2-Dihydroxy-3-nitroanthraquinonePurity:98%Molecular weight:285.21g/mol1,2-Dihydroxy-3-nitroanthraquinone
CAS:<p>1,2-Dihydroxy-3-nitroanthraquinone is a chemical compound that is an inorganic pigment with an orange color. It has been used as a dyestuff and as a reagent in organic synthesis. The compound is obtained by the oxidation of 1,2-dihydroxynaphthalene with nitric acid and hydrogen peroxide. 1,2-Dihydroxy-3-nitroanthraquinone has been studied electrochemically using cyclic voltammetry. Hydrogen bonding to the hydroxyl groups on the ring structure increases its activation energy. Inorganic reactions include protonation and alpha-synuclein formation, which can be prevented by adding ammonium acetate or sodium bicarbonate. Optical properties are also affected by pH and concentration gradients. This chemical has hydrophilic properties due to its high content of oxygen atoms and dry weight is determined through gravimetric analysis.<br>Synonyms</p>Formula:C14H7NO6Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:285.21 g/mol1,2-Dihydroxy-3-nitroanthraquinone
CAS:Controlled Product<p>Applications 1,2-Dihydroxy-3-nitroanthraquinone (cas# 568-93-4) is useful for the development of allosteric PGAM1 inhibitors that are effective at suppressing the proliferation of pancreatic ductal adenocarcinoma cells.<br>References Wen, C. L., et al.: Proc. Natl. Acad. Sci. U.S.A, 116, 23264 (2019)<br></p>Formula:C14H7NO6Color and Shape:YellowMolecular weight:285.21



