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3-Isobutylcyclohexene

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Identification
Molecular formula
C10H18
CAS number
10253-95-5
IUPAC name
3-isobutylcyclohexene
State
State

At room temperature, 3-isobutylcyclohexene exists as a liquid.

Melting point (Celsius)
-51.00
Melting point (Kelvin)
222.15
Boiling point (Celsius)
171.70
Boiling point (Kelvin)
444.90
General information
Molecular weight
136.24g/mol
Molar mass
136.2380g/mol
Density
0.8640g/cm3
Appearence

3-Isobutylcyclohexene is typically a colorless liquid. It may exhibit a mild aromatic odor depending on its purity and specific concentration.

Comment on solubility

Solubility of 3-isobutylcyclohexene

3-isobutylcyclohexene, a bicyclic compound, exhibits intriguing solubility properties that are influenced by its molecular structure. Understanding its solubility is essential for various applications in chemistry and engineering.

Solubility Characteristics

Considering its hydrophobic character, 3-isobutylcyclohexene is expected to demonstrate:

  • Low Water Solubility: Due to the absence of polar functional groups, 3-isobutylcyclohexene is not soluble in water.
  • Solubility in Organic Solvents: This compound is generally soluble in nonpolar and weakly polar organic solvents such as:
    • Cyclohexane
    • Toluene
    • Hexane

Moreover, it's worth noting that the degree of solubility can be influenced by factors such as:

  • Temperature: Increased temperature often leads to enhanced solubility in organic solvents.
  • Molecular Interactions: Interactions between solute and solvent molecules can greatly affect solubility behavior.

In summary, while it is not soluble in water, 3-isobutylcyclohexene finds compatibility with a range of organic solvents, illustrating the fundamental principles of solubility governed by molecular structure and polarity.

Interesting facts

Exploring 3-Isobutylcyclohexene

3-Isobutylcyclohexene is an intriguing organic compound that belongs to the class of cyclic alkenes. Here are some fascinating insights into this compound:

  • Cyclic Structure: The presence of a cyclohexene ring gives this compound unique properties compared to its acyclic counterparts. Cyclic structures often exhibit distinctive reactivity patterns and stereochemistry.
  • Isobutyl Group: The isobutyl substituent on the cyclohexene enhances the complexity of the molecule, leading to interesting steric effects that can influence its reactivity and interactions with other compounds.
  • Applications: 3-Isobutylcyclohexene can serve as a valuable intermediate in organic synthesis. Its derivatives may be used in the production of fragrances, agrochemicals, and other industrial chemicals.
  • Reactivity: As an alkene, 3-isobutylcyclohexene is likely to participate in various addition reactions. This characteristic makes it a potential candidate for polymerization or functional group transformation.
  • Nature of Alkenes: Alkenes are known for their ability to undergo reactions such as hydrogenation, halogenation, and oxidation, making them versatile in chemical synthesis.

The study of 3-isobutylcyclohexene offers a glimpse into the fascinating realm of organic chemistry, illustrating how the structure of a compound can drastically influence its properties and applications in scientific and industrial contexts.

Synonyms
Cyclohexene, 3-isobutyl-
Cyclohexene, 3-(2-methylpropyl)-
4104-56-7
3-(2-Methylpropyl)-cyclohexene
3-Isobutylcyclohexene-1
3-Isobutyl-1-cyclohexene
3-(2-Methylpropyl)cyclohex-1-ene
3-isobutylcyclohex-1-ene
3-(2-METHYLPROPYL)CYCLOHEXENE
3-(2-Methylpropyl)-1-cyclohexene
CHEBI:88554
3-(2-methyl-propyl)-cyclohexene
DTXSID00961400
NVLNRIBMCIJLQD-UHFFFAOYSA-N
Q27160445