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5-Methylcyclopenta-1,3-diene

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Identification
Molecular formula
C6H8
CAS number
1120-56-5
IUPAC name
5-methylcyclopenta-1,3-diene
State
State

At room temperature, it is a liquid. It is stable under ordinary conditions of use and storage.

Melting point (Celsius)
-111.00
Melting point (Kelvin)
162.15
Boiling point (Celsius)
103.00
Boiling point (Kelvin)
376.15
General information
Molecular weight
80.13g/mol
Molar mass
80.1270g/mol
Density
0.8455g/cm3
Appearence

5-Methylcyclopenta-1,3-diene is a colorless liquid. It has a characteristic sweet odor, typical of many hydrocarbons.

Comment on solubility

Solubility of 5-methylcyclopenta-1,3-diene

5-methylcyclopenta-1,3-diene (C6H8) exhibits interesting solubility characteristics that can be essential for its practical applications. Here are key points regarding its solubility:

  • Hydrocarbon Nature: Being a hydrocarbon compound, 5-methylcyclopenta-1,3-diene is expected to be non-polar, which influences its solubility behavior.
  • Solvent Compatibility: This compound generally shows good solubility in non-polar solvents such as hexane, benzene, and toluene, while being poorly soluble in polar solvents such as water.
  • Room Temperature Behavior: At room temperature, 5-methylcyclopenta-1,3-diene is likely to dissolve readily in an organic phase, allowing for its use in various chemical processes.
  • Essential Considerations: When conducting experiments or applications, it is crucial to consider the choice of solvents due to the solubility profile, as it can significantly affect the outcomes of reactions involving this compound.

In summary, the solubility of 5-methylcyclopenta-1,3-diene is heavily influenced by its non-polar nature, making it more compatible with non-polar solvents while exhibiting limited solubility in polar environments. Understanding these solubility traits is essential for its effective utilization in scientific applications.

Interesting facts

Interesting Facts about 5-Methylcyclopenta-1,3-diene

5-Methylcyclopenta-1,3-diene is a fascinating compound in the realm of organic chemistry, known for its unique structure and reactivity. Here are some engaging insights about this intriguing compound:

  • Cyclopentadiene Derivative: This compound is derived from cyclopentadiene, a key building block in synthetic organic chemistry. Its structure includes a methyl group which can influence its properties and reactivity.
  • Applications: It is used in organic synthesis, particularly in the manufacture of various polymers, resins, and other organic materials.
  • Reactivity: Due to the presence of diene functionalities, 5-methylcyclopenta-1,3-diene can participate in Diels-Alder reactions, making it a valuable intermediate in creating complex organic molecules.
  • Isomerism: The compound exhibits interesting isomeric forms related to its diene structure, leading to various reactivity profiles and potential applications.
  • Combustion Behavior: Understanding the combustion properties of this compound can provide insights into its safety profile and environmental impact, especially in industrial settings.
  • Symmetry and Strain: The molecule possesses unique symmetry characteristics and potential ring strain due to its cyclic configuration, adding to its chemical intrigue.

In summary, 5-methylcyclopenta-1,3-diene is not merely a structural curiosity but a compound with significant relevance in both academic research and industrial applications. Its characteristics underscore the importance of understanding the implications of structure on reactivity in the field of chemistry. As one prominent chemist once said, "The structure of a compound is the key to its properties."

Synonyms
5-Methyl-1,3-cyclopentadiene
5-methylcyclopenta-1,3-diene
5-Methylcyclopentadiene
1,3-Cyclopentadiene, 5-methyl-
X1DWO24VEA
UNII-X1DWO24VEA
DTXSID7048035
CYCLOPENTADIENE, 5-METHYL-
DTXCID3028009
qvrbgkyllclchl-uhfffaoysa-n
96-38-8
SCHEMBL312784
SCHEMBL336846
SCHEMBL1004054
SCHEMBL27312775
SCHEMBL28073405
CHEBI:229345
Q22077211