CAS 548-39-0
:Phenalenone
Description:
Phenalenone, with the CAS number 548-39-0, is an organic compound characterized by its polycyclic aromatic structure. It features a fused ring system comprising three benzene rings and a ketone functional group, which contributes to its unique chemical properties. Phenalenone is typically a yellowish to brown solid at room temperature and is known for its ability to undergo various chemical reactions, including oxidation and reduction. It exhibits fluorescence, making it of interest in photochemical applications. The compound is relatively stable under standard conditions but can be sensitive to light and heat, which may lead to degradation. Phenalenone is utilized in organic synthesis and has potential applications in materials science, particularly in the development of organic semiconductors and dyes. Its solubility varies depending on the solvent, and it is generally more soluble in organic solvents than in water. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.
Formula:C13H8O
InChI:InChI=1/C13H8O/c14-12-8-7-10-4-1-3-9-5-2-6-11(12)13(9)10/h1-8H
InChI key:InChIKey=WWBGWPHHLRSTFI-UHFFFAOYSA-N
SMILES:O=C1C2=C3C(C=C1)=CC=CC3=CC=C2
Synonyms:- 1H-Benzonaphthen-1-one
- 1H-phenalen-1-one
- 7-Perinaphthenone
- NSC 150161
- Perinaphthalenone
- Phenalen-1-One
- Phenalenone
- Phenalone
- Perinaphthenone
- peri-Naphthindone
- Perinaphthenone,97%
- Perinaphthenon
- Perinaphthanone
- peri-Naphthindenone
- See more synonyms
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Found 5 products.
Perinaphthenone
CAS:PerinaphthenoneFormula:C13H8OPurity:95%Color and Shape: orange solidMolecular weight:180.20g/mol1H-Phenalen-1-one
CAS:Controlled Product<p>Applications 1H-Phenalen-1-one (CAS# 548-39-0) is a useful research chemical compound.<br></p>Formula:C13H8OColor and Shape:Yellow To Dark OrangeMolecular weight:180.202Perinaphthenone
CAS:<p>Perinaphthenone is a potent inducer of the benzalkonium chloride-resistant (BAR) phenotype. It is an antimicrobial agent that acts by inhibiting the polymerase chain reaction (PCR), which is essential for DNA replication. The mechanism of action of perinaphthenone involves hydroxyl group transfer reactions, which are responsible for its potent inducers of BAR. In addition, perinaphthenone has been shown to inhibit mitochondrial membrane potential and reactive oxygen species generation in human neutrophils, making it a promising drug candidate for infectious diseases. <br>The high values achieved by this molecule suggest that it may be useful as a model system to study the molecular basis of antimicrobial resistance.</p>Formula:C13H8OPurity:Min. 95%Molecular weight:180.2 g/mol




