9,10-Phenanthrenequinone

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Catalog Number ACM84117-1
CAS 84-11-7
Structure {[CurrentData.Name]}
IUPAC Name phenanthrene-9,10-dione
Synonyms 9,10-Phenanthrenedione
Molecular Weight 208.21
Molecular Formula C14H8O2
Canonical SMILES O=C1C(=O)C2=C(C=CC=C2)C2=CC=CC=C12
Inchi InChI=1S/C14H8O2/c15-13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)14(13)16/h1-8H
InChIKey YYVYAPXYZVYDHN-UHFFFAOYSA-N
Boiling Point 360.0±0.0 °C at 760 mmHg
Melting Point 209-212 °C(lit.)
Flash Point 163.1±4.4 °C
Purity 98%
Density 1.3±0.1 g/cm3
Solubility 3.60e-05 M;Solubility in water: 0.4 mg/mL;Solubility in ethanol: 1 mg/mL; solubility in ethylene glycol methyl ether: 7 mg/mL;Soluble in benzene, ether, glacial acetic acid, hot alcohol;Soluble in sulfuric acid
Appearance Powder
Application 9,10-Phenanthrenequinone is a burnt-orange powder that serves a multitude of functional roles. It is notably utilized for high-quality passivation on silicon (100) surfaces, ensuring the protection and stabilization of this material. Additionally, as a member of the phenanthrenes, 9,10-Phenanthrenequinone is found abundantly in diesel exhaust particles, contributing to air pollution and exhibiting cytotoxic effects both in vitro and in vivo. This compound plays a significant role in cytotoxicity by generating reactive oxygen species through redox cycling, while also reducing glutathione expression, vital for detoxification. The versatile reactivity of 9,10-Phenanthrenequinone extends to its interactions with various ketones under FeCl3 catalysis, producing diverse furan-annulated products. Through processes involving aldol condensation, dehydration, and cyclization, reaction with ketones like cycloheptanone and cyclooctanone also yields complex furan structures, showcasing its utility in synthetic chemistry.
Storage room temp
Refractive Index 1.659

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