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5-Ethylnon-3-en-2-one

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Identification
Molecular formula
C11H20O
CAS number
None
IUPAC name
5-ethylnon-3-en-2-one
State
State

At room temperature, 5-ethylnon-3-en-2-one is a liquid. It has a moderate volatility typical of medium-chain length ketones, indicating its liquid state across a range of typical environmental temperatures.

Melting point (Celsius)
-65.00
Melting point (Kelvin)
208.15
Boiling point (Celsius)
215.50
Boiling point (Kelvin)
488.65
General information
Molecular weight
154.28g/mol
Molar mass
154.2500g/mol
Density
0.8053g/cm3
Appearence

5-Ethylnon-3-en-2-one is a clear, colorless liquid with a characteristic ketone-like odor. Its liquid state is consistent with many other ketones that are used in organic synthesis and flavor industries.

Comment on solubility

Solubility of 5-ethylnon-3-en-2-one (C11H20O)

5-ethylnon-3-en-2-one, also known as an α,β-unsaturated ketone, exhibits interesting solubility characteristics due to its molecular structure.

Solubility Characteristics

In general, the solubility of this compound can be summarized as follows:

  • Polar Solvents: 5-ethylnon-3-en-2-one is capable of dissolving in polar solvents, exemplifying its affinity for solvents such as ethanol and methanol.
  • Non-polar Solvents: It also shows compatibility with non-polar solvents like hexane and dichloromethane, indicating that its hydrophobic properties allow it to mix well in less polar environments.

This dual solubility behavior implies that the compound could be utilized in a variety of chemical reactions and applications, depending on the solvent environment. As a rule of thumb, compounds with larger hydrocarbon portions like those in 5-ethylnon-3-en-2-one typically enhance solubility in non-polar media.

Key Takeaway

In summary, 5-ethylnon-3-en-2-one's solubility profile provides significant versatility, making it an intriguing subject for further research and application in organic chemistry.

Interesting facts

Interesting Facts about 5-Ethylnon-3-en-2-one

5-Ethylnon-3-en-2-one, a compound known for its intriguing characteristics, is widely recognized in the field of synthetic organic chemistry.

Key Characteristics:

  • Functionality: This compound features a concerted functional structure that includes both a ketone and an alkene, making it a highly reactive species in various chemical reactions.
  • Applications: 5-Ethylnon-3-en-2-one is often utilized as a building block in the synthesis of more complex organic molecules. It serves as an intermediate in the production of flavors, fragrances, and pharmaceutical ingredients.
  • Reactivity: The presence of the double bond (alkene) in 5-Ethylnon-3-en-2-one allows it to undergo addition reactions, contributing to its versatility in synthesis.

Chemical Significance:

This compound is particularly noteworthy due to its potential applications in the industry. It is a key player in the development of:

  • Natural product synthesis
  • Organic photonic materials
  • Advanced polymer composites

A Quote to Ponder:

As famed chemist Linus Pauling once said, "The best way to have a good idea is to have a lot of ideas." The versatility of compounds like 5-ethylnon-3-en-2-one exemplifies how creative chemical synthesis can lead to innovative solutions in various fields.

Overall, 5-ethylnon-3-en-2-one represents a fascinating intersection of functionality and reactivity, holding great promise for future discoveries and applications in chemistry.

Synonyms
5-Ethylnon-3-en-2-one
233-379-8
10137-90-3
5-Athyl-3-nonen-2-on
SCHEMBL6065132
SWBGUNASIKSCCO-UHFFFAOYSA-N
AT44182
NS00044719