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9-Fluorononanal

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Identification
Molecular formula
C9H17FO
CAS number
50783-56-1
IUPAC name
9-fluorononanal
State
State

At room temperature, 9-Fluorononanal is in a liquid state. It is not very volatile and has a relatively higher boiling point than many short-chain aldehydes due to its longer carbon chain and fluorine substitution.

Melting point (Celsius)
-33.00
Melting point (Kelvin)
240.15
Boiling point (Celsius)
228.50
Boiling point (Kelvin)
501.65
General information
Molecular weight
160.23g/mol
Molar mass
160.2280g/mol
Density
0.9365g/cm3
Appearence

9-Fluorononanal is typically a clear, colorless to pale yellow liquid. It is similar in appearance to other aldehydes and exhibits a strong, often pungent odor characteristic of lower aliphatic aldehydes.

Comment on solubility

Solubility of 9-Fluorononanal

9-Fluorononanal, with the chemical formula C9H17FO, belongs to a class of compounds known as aldehydes. Its solubility profile can be intriguing and varies depending on the solvent used. Here are some key points about the solubility of this compound:

  • Solvent Polarity: 9-Fluorononanal is expected to be more soluble in polar organic solvents such as acetone or ethanol compared to non-polar solvents.
  • Hydrophobic Character: As an aldehyde with a longer carbon chain, it exhibits some hydrophobic properties, making it less soluble in water.
  • Functional Group Influence: The presence of the fluoro group can influence hydrogen bonding and interaction with various solvents, potentially increasing the solubility in specific cases.
  • Temperature Effects: Like many organic compounds, its solubility may increase with temperature; thus, heating the solvent might improve the dissolution rate.

In summary, while 9-fluorononanal shows variable solubility characteristics, it is generally more soluble in polar organic solvents rather than in water. Understanding these solubility dynamics is essential for applications in synthesis and formulation processes.

Interesting facts

Interesting Facts about 9-Fluorononanal

9-Fluorononanal is a fascinating chemical compound that has garnered attention in various fields, particularly in organic synthesis and medicinal chemistry. Here are some intriguing aspects of this compound:

  • Functional Group: This compound contains an aldehyde group, which is known for its reactivity in organic reactions. Aldehydes like 9-fluorononanal are often used in the synthesis of more complex molecules.
  • Fluorine Substitution: The presence of a fluorine atom at the 9th position is significant. Fluorine can influence a molecule's properties, such as its polarity and reactivity. This makes 9-fluorononanal a valuable compound in the design of pharmaceuticals and agrochemicals.
  • Applications in Organic Synthesis: 9-Fluorononanal may serve as an important intermediate in the synthesis of various biologically active compounds. Chemists leverage its unique structure to build complex, multi-functionalized molecules.
  • Research Importance: Studies involving 9-fluorononanal are pivotal in understanding the behavior of fluorinated compounds in biological systems. Researchers are continually exploring how the incorporation of fluorine affects molecular interactions and biological activity.
  • Green Chemistry: The synthesis of 9-fluorononanal can sometimes be aligned with green chemistry principles, employing safer and more sustainable methods to create fluorinated products. This is particularly relevant in modern chemical practices.

In summary, 9-fluorononanal is more than just a simple aldehyde. It plays a significant role in advancing the field of organic chemistry, particularly in the synthesis of innovative compounds with potential therapeutic applications. As you delve deeper into this compound, you will discover its multifaceted impact on both science and industry.

Synonyms
9-Fluorononanal
463-25-2
NONANAL, 9-FLUORO-
BRN 1703280
DTXSID40196794