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4-fluoranthen-8-yl-4-oxo-butanoic acid

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Identification
Molecular formula
C18H12O3
CAS number
16631-30-8
IUPAC name
4-fluoranthen-8-yl-4-oxo-butanoic acid
State
State

At room temperature, 4-fluoranthen-8-yl-4-oxo-butanoic acid is in a solid state. It is typically handled as a powder or crystalline substance. The compound's solid form is stable under normal conditions when stored properly.

Melting point (Celsius)
159.00
Melting point (Kelvin)
432.15
Boiling point (Celsius)
371.00
Boiling point (Kelvin)
644.15
General information
Molecular weight
292.29g/mol
Molar mass
292.3100g/mol
Density
1.3000g/cm3
Appearence

4-Fluoranthen-8-yl-4-oxo-butanoic acid typically appears as a crystalline solid. The coloration can vary from a pale yellow to a white powder, depending on the purity and specific preparation of the compound. As a solid, it readily absorbs moisture from the air, which may affect its appearance.

Comment on solubility

Solubility of 4-fluoranthen-8-yl-4-oxo-butanoic acid

The solubility of 4-fluoranthen-8-yl-4-oxo-butanoic acid can be influenced by several factors, including its molecular structure and functional groups. Understanding this compound's solubility characteristics is essential for applications in various chemical processes. Here are some key points to consider:

  • Polarity: The presence of polar functional groups often enhances solubility in polar solvents, while nonpolar sections may prefer nonpolar solvents.
  • Hydrogen Bonding: This compound may participate in hydrogen bonding, significantly affecting its solubility in water and other solvents.
  • Solvent Compatibility: Solubility behaviors can vary with solvent type. Common solvents might include water, ethanol, or organic solvents depending on the polarity of the compound.
  • Temperature Effect: The solubility of many organic compounds, including 4-fluoranthen-8-yl-4-oxo-butanoic acid, generally increases with temperature.

In summary, the solubility of 4-fluoranthen-8-yl-4-oxo-butanoic acid is a complex interplay of its chemical structure, interactions with solvents, and external conditions. As the saying goes, *"like dissolves like,"* making a thorough understanding of this compound's properties essential for its effective application in chemical formulations.

Interesting facts

Interesting Facts about 4-Fluoranthen-8-yl-4-oxo-butanoic Acid

4-Fluoranthen-8-yl-4-oxo-butanoic acid is a fascinating compound garnering attention in various fields of research. Here's a glimpse into what makes this compound particularly intriguing:

  • Structure and Function: This compound features a unique structure that combines a fluoranthene moiety with a ketone and carboxylic acid group, which contributes to its reactivity and biological activity. The fluoranthene part provides a polycyclic aromatic hydrocarbon backbone, making it significant in studies related to organic electronics and material science.
  • Biological Relevance: Compounds like 4-fluoranthen-8-yl-4-oxo-butanoic acid may exhibit various biological activities, including antitumor properties. Research into such compounds often highlights their potential use in pharmaceuticals, where understanding their mechanism of action can lead to novel drug candidates.
  • Suitability for Synthesis: Due to its diverse functional groups, this compound serves as a versatile intermediate in organic synthesis. It could be used in the development of more complex organic molecules, further enriching the field of synthetic chemistry.
  • Environmental Impact: As a derivative of polycyclic aromatic hydrocarbons, it invites a discussion on environmental chemistry, particularly concerning its persistence and degradation in the environment. Understanding these properties aids in assessing the ecological risks associated with similar compounds.
  • Research Frontiers: Scientists are continually exploring the potential applications of compounds like 4-fluoranthen-8-yl-4-oxo-butanoic acid in fields such as nanotechnology, materials science, and the development of electronic devices. The ongoing research investigates its electronic, thermal, and optical properties.

As with many chemical compounds, the study of 4-fluoranthen-8-yl-4-oxo-butanoic acid not only broadens our understanding of organic chemistry but also pushes the boundaries of innovation in diverse scientific disciplines. The journey to unlock the potential of such compounds is an exciting realm for chemists and researchers alike.

Synonyms
FLORANTYRONE
Fluorantyrone
Zanchol
Florantirona
Florantyron
Fluochol
Florantyronum
Cistoplex
Idrobil
Idroepar
Anchol
Bilyn
Kanchol
Florantyrone [INN:BAN]
UNII-UZ5LMI200P
Florantyronum [INN-Latin]
Florantirona [INN-Spanish]
UZ5LMI200P
HSDB 3331
beta-(8-Fluoranthoyl)propionic acid
EINECS 208-279-2
gamma-Oxo-8-fluoranthenebutyric acid
FLORANTYRONE [MI]
FLORANTYRONE [INN]
gamma-Oxo-8-fluoranthenebutanoic acid
4-(FLUORANTHEN-8-YL)-4-OXOBUTANOIC ACID
beta-(8-Fluoranthyloyl)propionic acid
FLORANTYRONE [HSDB]
.gamma.-Oxo-8-fluoranthenebutyric acid
8-Fluoranthenebutyric acid, gamma-oxo-
SC 1674
4-(8-Fluoranthenyl)-4-oxobutyric acid
8-Fluoranthenebutanoic acid, gamma-oxo-
FLORANTYRONE [MART.]
FLORANTYRONE [WHO-DD]
DTXSID3023055
8-Fluoranthenebutanoic acid, .gamma.-oxo-
Florantyronum (INN-Latin)
Florantirona (INN-Spanish)
FLORANTYRONE (MART.)
florantirone
flurantyron
DTXCID803055
8-FLUORATHENEBUTANOIC ACID, GAMMA-OXO-
208-279-2
qobaoscolagpki-uhfffaoysa-n
519-95-9
4-fluoranthen-8-yl-4-oxobutanoic acid
SCHEMBL1643339
CHEMBL2106357
CHEBI:135279
DB08975
4-(8-Fluoranthenyl)-4-oxobutanoic acid #
NS00032399
Q5460488