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3-Methylcyclopentene

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Identification
Molecular formula
C6H10
CAS number
1120-62-3
IUPAC name
3-methylcyclopentene
State
State

At room temperature, 3-Methylcyclopentene is in a liquid state. It is a volatile compound that can be easily vaporized.

Melting point (Celsius)
-136.00
Melting point (Kelvin)
137.15
Boiling point (Celsius)
90.00
Boiling point (Kelvin)
363.15
General information
Molecular weight
82.15g/mol
Molar mass
82.1460g/mol
Density
0.7395g/cm3
Appearence

3-Methylcyclopentene is a colorless, clear liquid with a noticeable hydrocarbon odor. It is typically handled in its liquid form and can emit flammable vapors.

Comment on solubility

Solubility of 3-methylcyclopentene

3-methylcyclopentene, with the chemical formula C6H10, is an organic compound that presents unique solubility characteristics due to its specific structure and degree of saturation. Here are some key points regarding its solubility:

  • Solvent Compatibility: 3-methylcyclopentene is primarily soluble in non-polar solvents such as hexane and toluene. This is attributed to its hydrocarbon nature, which aligns well with the properties of non-polar solvents.
  • Water Solubility: This compound exhibits minimal solubility in water. As a non-polar organic compound, it does not readily interact with polar water molecules.
  • Temperature Effects: Increasing the temperature can enhance the solubility of 3-methylcyclopentene in organic solvents, potentially due to reduced viscosity and increased molecular movement.

In summary, if you are experimenting with 3-methylcyclopentene or considering it for practical applications, keep in mind its limited solubility in water and favorable solubility in non-polar organic solvents. Understanding these solubility traits will aid in appropriate handling and usage in various chemical processes.

Interesting facts

Interesting Facts About 3-Methylcyclopentene

3-Methylcyclopentene is an intriguing chemical compound that draws interest for several reasons:

  • Cyclic Structure: This compound features a five-membered ring, characteristic of cyclopentene, which contributes to its unique properties.
  • Unsaturation: As an alkene, it contains a double bond, making it particularly reactive and versatile in various chemical reactions.
  • Substituent Effects: The methyl group at the 3-position offers interesting substitution patterns and influences the reactivity, making this compound an excellent candidate for mechanistic studies.
  • Applications: Due to its structural properties, 3-methylcyclopentene is explored in the synthesis of more complex organic compounds and can serve as a useful intermediate in organic chemistry.

Interestingly, this compound isn't just a fascinating subject for study; it also showcases the beauty of organic chemistry through its ability to participate in various reactions, such as Diels-Alder reactions, which are pivotal in constructing complex molecular architectures.

As noted by chemists, "Understanding the behavior of small cyclic structures like 3-methylcyclopentene can lead to insights in reactivity and synthetic strategy."

In summary, 3-methylcyclopentene exemplifies how simple structural variations in organic compounds can lead to significant implications in chemical behavior and application.

Synonyms
3-METHYLCYCLOPENTENE
Cyclopentene, 3-methyl-
3-methylcyclopent-1-ene
3-Methyl-1-cyclopentene
3-methylcyclopentene-1
3-methyl-cyclopentene
EINECS 214-315-8
DTXSID80870844
DTXCID80818529
214-315-8
cxozqhpxkpdqgt-uhfffaoysa-n
1120-62-3
(RS)-3-Methylcyclopentene; 3-Methylcyclopentene; 5-Methylcyclopentene; R,S-3-Methylcyclopentene
3-Methyl-1-cyclopentene #
CHEBI:177575
MFCD00053260
AKOS006283775
DB-241099
NS00045149
EN300-1663070