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1,2,3-trimethylcyclohexane

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Identification
Molecular formula
C9H18
CAS number
620-41-5
IUPAC name
1,2,3-trimethylcyclohexane
State
State

Liquid at room temperature.

Melting point (Celsius)
-86.00
Melting point (Kelvin)
187.15
Boiling point (Celsius)
162.00
Boiling point (Kelvin)
435.15
General information
Molecular weight
126.24g/mol
Molar mass
126.2390g/mol
Density
0.8670g/cm3
Appearence

Colorless liquid

Comment on solubility

Solubility of 1,2,3-trimethylcyclohexane

The solubility of 1,2,3-trimethylcyclohexane can be quite intriguing, given its unique structure and properties. As an organic compound, it primarily exhibits non-polar characteristics, which greatly influence its solubility behavior. Here are some key aspects of its solubility:

  • Non-polar Nature: Due to its cyclic structure and lack of polarity, 1,2,3-trimethylcyclohexane is expected to be soluble in non-polar solvents.
  • Solvent Compatibility: Common solvents that can dissolve this compound include:
    • Hexane
    • Benzene
    • Toluene
  • Poor Solubility in Polar Solvents: Conversely, it will have poor solubility in polar solvents such as:
    • Water
    • Ethanol
    • Acetone

In summary, the solubility of 1,2,3-trimethylcyclohexane can be succinctly encapsulated by the phrase: "Like dissolves like." This principle highlights the importance of considering both polarity and solvent choice when evaluating the solubility of such a compound.

Interesting facts

Interesting Facts about 1,2,3-Trimethylcyclohexane

1,2,3-Trimethylcyclohexane is a fascinating compound that belongs to the family of cyclic hydrocarbons, exhibiting unique structural and chemical properties. Here are some noteworthy aspects of this compound:

  • Structure: The molecular structure of 1,2,3-trimethylcyclohexane features a cyclohexane ring with three methyl groups attached at the 1, 2, and 3 positions. This specific arrangement leads to interesting stereochemical considerations and contributes to its overall stability.
  • Isomerism: The compound showcases several stereoisomers due to the presence of multiple chiral centers. It is a great example for students studying organic chemistry as it provides insights into concepts such as conformation and isomerism.
  • Source: 1,2,3-Trimethylcyclohexane can be derived from the natural degradation of terpenes, which are abundant in essential oils and plant resins. This makes it significant in the context of organic synthesis and material science.
  • Applications: Though not as widely known as other hydrocarbons, the compound serves as an important building block in organic compounds used in pharmaceuticals and fragrances. Its unique properties can be harnessed for creating various derivatives.
  • Research Potential: The study of 1,2,3-trimethylcyclohexane can lead to insights regarding the stability of cycloalkanes and their derivatives. Such research can contribute to advancements in synthetic strategies and material development.

In summary, 1,2,3-trimethylcyclohexane is not just another cyclic hydrocarbon; it is a compound rich in learning opportunities for students and researchers alike. Its intriguing structure and potential applications make it a significant compound in the field of chemistry.

Synonyms
1,2,3-TRIMETHYLCYCLOHEXANE
1678-97-3
EINECS 216-838-7
DTXSID10862732
DTXCID00811456
216-838-7
Cyclohexane, 1,2,3-trimethyl-
cis,cis,cis-1,2,3-Trimethylcyclohexane
1678-81-5
Cyclohexane, 1,2,3-trimethyl-, (1.alpha.,2.alpha.,3.alpha.)-
1,2,3-Trimethylcyclohexane,cis
cis-1,2,3-Trimethylcyclohexane
1,cis-2,cis-3-Trimethylcyclohexane
Cyclohexane, 1,2,3-trimethyl-, cis
MFCD00045496
1,2,3-Trimethylcyclohexane-, (1.alpha.,2.alpha.,3.alpha.)- #
DB-043719
NS00046104
T0824
T71900