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4,4-Dimethylcyclohexene

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Identification
Molecular formula
C8H14
CAS number
1678-62-4
IUPAC name
4,4-dimethylcyclohexene
State
State

At room temperature, 4,4-dimethylcyclohexene is a liquid.

Melting point (Celsius)
-80.00
Melting point (Kelvin)
193.15
Boiling point (Celsius)
131.10
Boiling point (Kelvin)
404.25
General information
Molecular weight
110.20g/mol
Molar mass
110.1960g/mol
Density
0.8180g/cm3
Appearence

4,4-Dimethylcyclohexene is a colorless liquid.

Comment on solubility

Solubility of 4,4-Dimethylcyclohexene

4,4-Dimethylcyclohexene, with the chemical formula C10H18, is an organic compound characterized by its cyclohexene structure with two methyl groups attached to the same carbon atom. When it comes to solubility, this compound exhibits some interesting behavior:

  • Solvent Preference: 4,4-Dimethylcyclohexene is generally more soluble in nonpolar solvents due to its hydrophobic characteristics, making it less soluble in polar solvents like water.
  • Hydrophobic Nature: The presence of the cyclohexene ring and methyl groups contributes to a significant degree of hydrophobicity, which limits its solubility in polar environments.
  • Uses in Organic Chemistry: Its solubility profile makes it useful in various organic reactions and as a solvent for other nonpolar compounds.

In essence, it is pivotal to recognize the importance of solvent choice when working with 4,4-dimethylcyclohexene. As a rule of thumb, nonpolar solvents will yield better solubility results, enhancing the compound's effectiveness in synthetic applications.

Interesting facts

Interesting Facts About 4,4-Dimethylcyclohexene

4,4-Dimethylcyclohexene is an intriguing compound within the broader family of cycloalkenes, notable for its unique structural properties and versatile applications in organic chemistry. Here are some fascinating aspects about this compound:

  • Cycloalkene Nature: As a member of the cycloalkene class, 4,4-dimethylcyclohexene features a cyclic structure with a double bond, contributing to its reactivity and chemical behavior.
  • Isomerism: The presence of multiple methyl groups on the cyclohexene ring allows for various isomeric forms. This molecular diversity can lead to different physical and chemical properties, making them useful in certain synthetic applications.
  • Reactivity: The double bond in 4,4-dimethylcyclohexene can participate in a range of chemical reactions, such as addition reactions. This characteristic makes it a subject of interest for chemists looking to create new compounds through various synthetic pathways.
  • Common Uses: The compound finds utility in organic synthesis, particularly in the formation of larger and more complex molecules. Its derivatives can be employed in pharmaceuticals, agrochemicals, and as intermediates in various chemical processes.
  • Synthetic Pathways: 4,4-Dimethylcyclohexene can be synthesized through several methods, with one common route involving the alkylation of cyclohexene. This showcases the compound’s versatility and the approachability of its synthetic methods.

In summary, 4,4-dimethylcyclohexene serves as a prime example of how structural properties influence chemical behavior and reactivity. The exploration of this compound not only advances our understanding of cycloalkenes but also opens up opportunities for innovative applications in chemical research and industry.

Synonyms
4,4-DIMETHYLCYCLOHEXENE
Cyclohexene, 4,4-dimethyl-
4,4-Dimethyl-1-cyclohexene
1-Cyclohexene, 4,4-dimethyl-
DTXSID00161468
NSC 134990
DTXCID6083959
DRORSPJLYCDESA-UHFFFAOYSA-N
14072-86-7
4,4-Dimethylcyclohex-1-ene
MT2HS4ZTL7
NSC-134990
NSC134990
Cyclohexene,4-dimethyl-
UNII-MT2HS4ZTL7
SCHEMBL196077
SCHEMBL284307
SCHEMBL755216
SCHEMBL4175758
SCHEMBL6589811
SCHEMBL10580183
AKOS006281263
EN300-314233