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Fluoren-2-yl chloroacetone

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Identification
Molecular formula
C15H11ClO
CAS number
122-69-0
IUPAC name
2-chloro-1-(9H-fluoren-2-yl)ethanone
State
State

At room temperature, Fluoren-2-yl chloroacetone is a solid. It is not very volatile and usually handled as a solid in laboratory settings.

Melting point (Celsius)
60.00
Melting point (Kelvin)
333.15
Boiling point (Celsius)
354.80
Boiling point (Kelvin)
627.95
General information
Molecular weight
230.69g/mol
Molar mass
230.6930g/mol
Density
0.5231g/cm3
Appearence

Fluoren-2-yl chloroacetone typically appears as a white to off-white crystalline solid. The compound is known for its distinctive aromatic structure, which contributes to its solid state at room temperature.

Comment on solubility

Solubility of 2-chloro-1-(9H-fluoren-2-yl)ethanone

The solubility of 2-chloro-1-(9H-fluoren-2-yl)ethanone can be considered within the context of its structural properties and intermolecular interactions. This compound exhibits a few noteworthy characteristics:

  • Polarity: The presence of the chloro group and the carbonyl functional group can impart some polarity to the molecule. Typically, compounds with higher polarity tend to have better solubility in polar solvents.
  • Hydrophobic Nature: The fluorenyl moiety is largely hydrophobic, which might limit its solubility in polar solvents while enhancing its solubility in non-polar organic solvents.
  • Common Solvents: Based on its structure, 2-chloro-1-(9H-fluoren-2-yl)ethanone is likely to be more soluble in solvents such as ethyl acetate, chloroform, and benzene due to their ability to minimize energetic penalties associated with solvation.

In summary, while 2-chloro-1-(9H-fluoren-2-yl)ethanone may display limited solubility in water due to its hydrophobic character, it is expected to dissolve readily in most organic solvents, making it versatile for use in various chemical applications.

Interesting facts

Interesting Facts about 2-chloro-1-(9H-fluoren-2-yl)ethanone

2-chloro-1-(9H-fluoren-2-yl)ethanone is an intriguing compound known for its unique structure and potential applications in various scientific fields. Here are some fascinating insights about this compound:

  • Fluorenyl Group: The presence of the 9H-fluoren-2-yl moiety gives this compound its interesting chemical properties, as fluorenes are often used in the development of optical materials and organic electronics.
  • Synthetic Applications: This compound has garnered interest in synthetic organic chemistry, particularly for its ability to serve as an intermediate in the creation of more complex molecules, potentially leading to novel compounds with interesting biological activities.
  • Reactivity: The chloro group in this structure enhances its reactivity. Chlorinated compounds are often valuable in cross-coupling reactions, making this compound a useful building block for constructing various organic frameworks.
  • Biological Significance: Compounds featuring the fluorenyl structure are known for their bioactivity. Research indicates they may exhibit properties such as antioxidant and anticancer activities, drawing attention for medicinal chemistry studies.
  • Potential in Materials Science: Due to its unique structure, 2-chloro-1-(9H-fluoren-2-yl)ethanone could be explored for applications in polymer science, specifically in the synthesis of light-emitting polymers which are essential in display technologies.

As researchers continue to explore the versatility and functionality of 2-chloro-1-(9H-fluoren-2-yl)ethanone, its potential uses in fields ranging from pharmaceuticals to materials science may pave the way for innovative discoveries. The combination of the chlorinated group and the fluorenyl moiety provides a fascinating avenue for exploration.

Synonyms
2-Chloroacetylfluorene
KETONE, CHLOROMETHYL 2-FLUORENYL
Fluorene, 2-(chloroacetyl)-
BRN 3093870
Ethanone, 2-chloro-1-(9H-fluoren-2-yl)-
24040-34-4
DTXSID10178789
RefChem:350456
DTXCID20101280
SCHEMBL10967373
AKOS010996521