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2-Phenyl-1-heptene

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Identification
Molecular formula
C13H18
CAS number
20464-04-4
IUPAC name
hept-2-enylbenzene
State
State

At room temperature, 2-Phenyl-1-heptene is a liquid.

Melting point (Celsius)
-67.00
Melting point (Kelvin)
206.15
Boiling point (Celsius)
217.00
Boiling point (Kelvin)
490.15
General information
Molecular weight
160.27g/mol
Molar mass
160.2660g/mol
Density
0.8160g/cm3
Appearence

2-Phenyl-1-heptene is a colorless to pale yellow liquid. It has a characteristic aromatic odor due to the presence of the phenyl group attached to the alkene structure. The compound is generally clear and may appear somewhat oily.

Comment on solubility

Solubility of Hept-2-enylbenzene

Hept-2-enylbenzene, with the chemical formula C11H14, exhibits interesting solubility characteristics due to its molecular structure. Being a hydrocarbon, it primarily showcases non-polar behavior, affecting its interaction with various solvents.

Solubility Characteristics:

  • Hept-2-enylbenzene is insoluble in water due to its hydrophobic nature.
  • It is, however, soluble in organic solvents such as alcohols, ethers, and aromatic hydrocarbons.
  • This compound tends to exhibit a greater affinity for non-polar solvents compared to polar solvents.

The solubility behaviors can be attributed to the presence of a long aliphatic chain and a benzene ring, which promotes compatibility with similar non-polar environments. As a general rule of thumb in chemistry, "like dissolves like," which means that hept-2-enylbenzene will better dissolve in solvents that share its non-polar characteristics.

In summary, when considering the solubility of hept-2-enylbenzene, one should remember its tendency to remain separate from aqueous solutions while thriving in organic solvents. This feature enhances its utility in various applications within organic chemistry.

Interesting facts

Hept-2-enylbenzene: A Unique Hydrocarbon

Hept-2-enylbenzene is an intriguing organic compound that falls under the category of aromatic hydrocarbons. This compound not only showcases the complexity of organic chemistry but also serves as an excellent example of how structural variations can lead to unique properties.

Key Characteristics

  • Structure: The compound features a benzene ring, which is a hallmark of aromatic stability, combined with a hept-2-enyl side chain. This structural combination results in interesting reactivity.
  • Alkene Conjugation: The presence of the double bond in the hept-2-enyl group introduces a level of reactivity, making it an important compound in organic synthesis and various chemical reactions.
  • Versatile Applications: Due to its unique chemical properties, hept-2-enylbenzene finds potential applications in the fields of pharmaceuticals, agrochemicals, and materials science.

Scientific Significance

This compound allows chemists to explore the dynamics of substituted aromatic systems, leading to advancements in the design of new materials. Its study can provide insights into:

  • Reaction Mechanisms: Understanding how hept-2-enylbenzene interacts with various reagents can shed light on broader reaction pathways.
  • Stability and Reactivity: Investigating the compound allows scientists to evaluate the balance between stability (due to the aromatic ring) and reactivity (due to the alkene).

Quote to Remember

"In the world of organic chemistry, even minor changes in structure can lead to significantly different compounds with unique properties and applications."

The exploration of hept-2-enylbenzene presents not just an opportunity for educational pursuits but also for innovation in synthetic methodologies. With ongoing research, this compound may unveil new pathways and applications, illustrating the beauty and complexity of organic chemistry.

Synonyms
2-HEPTENYLBENZENE
26447-63-2
SCHEMBL2656596
SCHEMBL4057587
SCHEMBL19031834
SCHEMBL27448664