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Benzo[a]phenalen-7-one

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Identification
Molecular formula
C17H10O
CAS number
208-72-6
IUPAC name
benzo[a]phenalen-7-one
State
State

At room temperature, Benzo[a]phenalen-7-one is a solid. It typically forms crystalline structures, which can be observed under appropriate conditions. The compound's solid state contributes to its stability and ease of handling in experimental settings.

Melting point (Celsius)
186.00
Melting point (Kelvin)
459.15
Boiling point (Celsius)
525.00
Boiling point (Kelvin)
798.15
General information
Molecular weight
230.27g/mol
Molar mass
230.2660g/mol
Density
1.3039g/cm3
Appearence

Benzo[a]phenalen-7-one typically appears as a yellow solid. Its coloration is due to the extended conjugation within its polycyclic aromatic framework, which also leads to its interesting photophysical properties.

Comment on solubility

Solubility of Benzo[a]phenalen-7-one

Benzo[a]phenalen-7-one, with the chemical formula C15H10O, presents intriguing characteristics regarding its solubility in various solvents. Solubility is an important aspect that can significantly affect the behavior and application of a compound in different environments.

Key Points on Solubility:

  • Polar vs. Non-Polar Solvents: Benzo[a]phenalen-7-one is generally more soluble in non-polar solvents due to its aromatic structure and lack of polar functional groups.
  • Common Solvents: It can be effectively dissolved in solvents such as benzene, toluene, and chloroform, which enhance its solubility due to similar polarities.
  • Water Solubility: The compound has limited solubility in water, as polar solvent interactions are not favorable owing to its non-polar nature.
  • Temperature Dependence: Solubility can vary with temperature, and it is often observed that higher temperatures may increase the solubility of organic compounds.

Understanding the solubility profile of benzo[a]phenalen-7-one is crucial for various applications, especially in organic synthesis and materials science. In summary, while this compound demonstrates limited solubility in polar environments, its solubility in non-polar solvents opens doors for potential uses in those domains. As the adage goes, “like dissolves like," meaning that the solvent's characteristics play a key role in solubility behavior.

Interesting facts

Interesting Facts about Benzo[a]phenalen-7-one

Benzoaphenalen-7-one is a fascinating member of the polycyclic aromatic hydrocarbons (PAHs) family, which often captures the attention of chemists due to its unique structural features and potential applications. Here are some key points that highlight its significance:

  • Complex Structure: The compound consists of multiple fused aromatic rings, contributing to its stability and unique electronic properties. Its structure allows for interesting interactions with other molecules.
  • Fluorescence: Benzoaphenalen-7-one exhibits fluorescence under UV light, making it a potential candidate for applications in chemical sensors and organic light-emitting diodes (OLEDs).
  • Environmental Impact: Like many PAHs, it is important to consider the environmental implications of benzoaphenalen-7-one, as compounds of this type can have health effects and be persistent pollutants.
  • Synthetic Routes: The synthesis of this compound provides an excellent opportunity for chemists to explore innovative methods in organic synthesis, demonstrating advancements in reaction techniques and catalyst development.
  • Research Application: Ongoing research on this compound focuses on its reactivity, interaction with biomolecules, and its uses in nanotechnology, where its electronic properties can be harnessed for various applications.

In conclusion, benzoaphenalen-7-one is more than just a chemical formula—it's a gateway to understanding complex molecular interactions and potential applications in modern chemistry. As research continues to unfold, this compound may reveal even more intriguing properties and uses, contributing to our growing body of knowledge in the realm of organic chemistry.

Synonyms
BENZANTHRONE
82-05-3
7H-Benz[de]anthracen-7-one
7H-benzo[de]anthracen-7-one
Benzanthrenone
MS-Benzanthrone
DYE, benzanthrone
Benzoanthrone
1,9-Benzanthrone
Mesobenzanthrone
benzo[a]phenalen-7-one
7H-Benz(de)anthracen-7-one
1,9-Benz-10-anthrone
7-Oxobenz(de)anthracene
7-Oxobenz[de]anthracene
7H-Benz(de)anthracene-7-one
7H-Benzo(de)anthracen-7-one
Benz(de)anthracen-7-one
NSC 5189
CCRIS 3173
NSC 631641
benz[de]anthracen-7-one
HSDB 5245
LP5P3RR8QN
EINECS 201-393-3
NSC-5189
BENZANTHRONE [MI]
BENZANTHRONE [HSDB]
NSC-631641
DTXSID8052566
NSC631641
7H-Benz[de]anthracene-7-one
UNII-LP5P3RR8QN
MSBenzanthrone
1,9Benzanthrone
MFCD00003585
7Oxobenz(de)anthracene
BENZANTHRONE DYE
7HBenz(de)anthracen7one
Spectrum2_000766
Spectrum3_001680
7HBenz(de)anthracene7one
7HBenzo(de)anthracen7one
SCHEMBL23838
BSPBio_003499
MLS002207268
SPECTRUM1505272
SPBio_000812
CHEMBL1607517
DTXCID5031139
CHEBI:93350
KBio3_002719
NSC5189
7H-BENZ(DE)ANTHRACENE-1-ONE
CCG-38994
STK662686
WLN: L C6666 1A Q IVJ
AKOS002319374
NCGC00095343-01
NCGC00095343-02
NCGC00178030-01
AS-56358
SMR001306791
B0019
CS-0070954
NS00003051
A51111
Q2075398
BRD-K76872913-001-02-8
F0001-2103
201-393-3
TETRACYCLO[7.7.1.0(2),?.0(1)(3),(1)?]HEPTADECA-1(17),2,4,6,9,11,13,15-OCTAEN-8-ONE