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3-Methyl-2-pent-2-enylcyclopent-2-en-1-one

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Identification
Molecular formula
C11H16O
CAS number
34103-58-5
IUPAC name
3-methyl-2-pent-2-enyl-cyclopent-2-en-1-one
State
State

At room temperature, this compound is in a liquid state.

Melting point (Celsius)
-99.90
Melting point (Kelvin)
173.25
Boiling point (Celsius)
258.00
Boiling point (Kelvin)
531.15
General information
Molecular weight
164.24g/mol
Molar mass
164.2440g/mol
Density
0.8622g/cm3
Appearence

The compound appears as a clear and colorless liquid. It may become slightly yellow on prolonged storage or exposure to light.

Comment on solubility

Solubility of 3-methyl-2-pent-2-enyl-cyclopent-2-en-1-one

The solubility of 3-methyl-2-pent-2-enyl-cyclopent-2-en-1-one in various solvents can be quite interesting due to its unique structure. Here are several key points regarding its solubility:

  • Polar Solvents: This compound is expected to have low solubility in polar solvents such as water due to its relatively non-polar hydrocarbon framework.
  • Non-Polar Solvents: In contrast, it is likely to be more soluble in non-polar solvents like hexane, benzene, or toluene, which can better accommodate its hydrophobic parts.
  • Temperature Dependence: Solubility can also vary with temperature, often increasing at elevated temperatures for non-polar solvents.
  • Functional Groups: The presence of double bonds and ketone functionality can influence solubility; these features may allow for some degree of interactions with polar solvents.

As a general observation, the structural characteristics and the environment of 3-methyl-2-pent-2-enyl-cyclopent-2-en-1-one will play a crucial role in determining its solubility.

In summary, while this compound may have limited solubility in water, its affinity for non-polar solvents allows for greater interactions, making it essential to consider the solvent choice in practical applications.

Interesting facts

Interesting Facts About 3-methyl-2-pent-2-enyl-cyclopent-2-en-1-one

3-methyl-2-pent-2-enyl-cyclopent-2-en-1-one is a fascinating compound with several noteworthy attributes that make it an intriguing subject of study in organic chemistry. Here are some compelling aspects of this compound:

  • Cyclic Structure: The compound features a cyclopentene moiety, which is a five-membered ring containing double bonds. This cyclic structure contributes to its unique chemical reactivity.
  • Isoprenoid Derivative: As a derivative of isoprene, it shares characteristics with many natural products and biochemicals, including essential oils and terpenes, making it relevant to the biosynthesis processes in various organisms.
  • Applications in Synthesis: The compound can act as a building block in organic synthesis, particularly in the creation of more complex molecules used in pharmaceuticals, agrochemicals, and natural products.
  • Possible Biological Activity: Many related compounds exhibit biological activity, such as anti-inflammatory and antimicrobial properties, suggesting that this compound may have potential medicinal applications, although more research is needed.
  • Importance in Flavor and Fragrance: Alkylated cyclopentenones are often studied for their scent profiles, which can enhance the olfactory attributes of perfumes and flavorings.

Overall, 3-methyl-2-pent-2-enyl-cyclopent-2-en-1-one presents a rich field for exploration in organic chemistry, with implications that cross over into fields such as biochemistry, pharmacology, and even materials science. The study of such compounds can lead to innovative applications and deeper understandings of chemical behavior in various contexts.

Synonyms
2-Cyclopenten-1-one, 3-methyl-2-(2Z)-2-pentenyl-
3-methyl-2-pent-2-enylcyclopent-2-en-1-one
3-Methyl-2-pent-2-enyl-cyclopent-2-enone
(EZ)-jasmone
(Z)-3-Methyl-2-(2-pentenyl)-2-cyclopentenone
3-methyl-2-(pent-2-en-1-yl)cyclopent-2-en-1-one
2-Cyclopenten-1-one, 3-methyl-2-(2Z)-2- pentenyl-
DTXSID50859404
AKOS028108957
SY036136
3- methyl-2-(2-pentenyl)-2-cylco-penten-1-one
Q65952186