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Terpinen-4-ol

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Identification
Molecular formula
C10H18O
CAS number
562-74-3
IUPAC name
5-isopropenyl-2-methyl-cyclohexanol
State
State

At room temperature, Terpinen-4-ol is in a liquid state.

Melting point (Celsius)
0.00
Melting point (Kelvin)
273.15
Boiling point (Celsius)
212.00
Boiling point (Kelvin)
485.15
General information
Molecular weight
154.25g/mol
Molar mass
154.2510g/mol
Density
0.9306g/cm3
Appearence

Terpinen-4-ol is a colorless to pale yellow liquid. It is often described to have a pleasant odor somewhat resembling that of eucalyptus or camphor.

Comment on solubility

Solubility of 5-isopropenyl-2-methyl-cyclohexanol

The solubility of 5-isopropenyl-2-methyl-cyclohexanol in various solvents can provide interesting insights into its chemical behavior. This compound, characterized by its organic structure, shows distinct solubility properties:

  • Polar Solvents: The presence of hydroxyl groups suggests that 5-isopropenyl-2-methyl-cyclohexanol is likely to be soluble in polar solvents such as water and alcohols due to hydrogen bonding.
  • Non-Polar Solvents: Conversely, its non-polar cyclohexane ring may enhance its solubility in non-polar solvents like hexane or benzene, which can favor interactions with hydrophobic sections of the molecule.
  • Temperature Influence: Temperature can significantly affect solubility, often increasing solubility in liquids as temperature rises, which contributes to varying solubility profiles in practical applications.

In summary, the multi-faceted nature of 5-isopropenyl-2-methyl-cyclohexanol's solubility makes it a candidate for diverse applications depending on the solvent environment. **Understanding these solubility characteristics is crucial in fields such as organic synthesis and formulation chemistry**, where solvent interactions dictate the success of reactions and product stability.

Interesting facts

Interesting Facts about 5-Isopropenyl-2-methyl-cyclohexanol

5-Isopropenyl-2-methyl-cyclohexanol, often referred to in the context of its unique structural attributes, is an intriguing compound in organic chemistry. This compound features a cyclic structure, which is a common motif in many natural products and pharmaceuticals. Here are some captivating aspects to consider:

  • Structural Characteristics: The presence of both isopropenyl and cyclohexanol groups plays a significant role in its behavior and reactivity. This unique combination allows it to potentially participate in a variety of chemical reactions.
  • Potential Biological Activity: Compounds like 5-isopropenyl-2-methyl-cyclohexanol are of interest in medicinal chemistry due to their possible biological activities. Similar compounds have been noted for their roles in fragrances and flavorings, which could indicate that this compound may also have similar applications.
  • Source Material: Many compounds within this family are derived from natural sources, leading researchers to explore the potential for synthetic methods to mimic nature’s complexity. This opens up pathways for sustainable synthesis or bioprospecting efforts for natural products.
  • Applications in Industry: The unique properties of this compound suggest that it may be used in the production of specialty chemicals or agrochemicals, where targeted reactivity is key.

The exploration of 5-isopropenyl-2-methyl-cyclohexanol continues to be a subject of research and interest due to its multifaceted role in chemistry and potential real-world applications.

As scientists and students engage with this compound, they may think, "How can natural inspiration lead us to new synthetic approaches?". The journey of understanding such compounds can lead to innovative solutions in various scientific fields.

Synonyms
Dihydrocarveol
1,6-Dihydrocarveol
2-methyl-5-(prop-1-en-2-yl)cyclohexanol
2-methyl-5-prop-1-en-2-ylcyclohexan-1-ol
5-Isopropenyl-2-methylcyclohexanol
CHEBI:50215
2-methyl-5-isopropenylcyclohexanol
(+-)-Dihydrocarveol
(+-)-trans-Dihydrocarveol
EINECS 253-755-5
DIHYDROCARVEOL [FHFI]
619-01-2
Cyclohexanol, 2-methyl-5-(1-methylethenyl)-
8-p-Menthen-2-ol
Neodihydrocarveol
6-Methyl-3-isopropenylcyclohexanol
2-Methyl-5-(1-methylethenyl)cyclohexanol
38049-26-2
Menth-8-en-2-ol
p-MENTH-8-EN-2-OL
2-methyl-5-(prop-1-en-2-yl)cyclohexan-1-ol
FEMA No. 2379
EINECS 210-575-1
a dihydrocarveol
1-Dihydrocarveol
Dihydro carveol neo
Neocarveol, dihydro-
(+/-)-dihydrocarveol
1-METHYL-4-ISOPROPENYL-2-CYCLOHEXANOL
SCHEMBL295511
CYCLOHEXANOL,2-METHYL-5-(1-METHYLETHENYL)-
GTPL6415
(1R,2S,5S)-neodihydrocarveol
DTXSID60862303
AKOS015906522
SB84645
DB-066237
DB-073026
NS00012229
p-Menth-8-en-2-ol, cis-1,2,trans-1,4-
C18017
G77216
Q1225152
5-Isopropenyl-2-methylcyclohexanol, (1.alpha.,2.alpha.,5.beta.)-
Cyclohexanol, 2-methyl-5-(1-methylethenyl)-, (1R,2S,5S)-rel-
Cyclohexanol, 2-methyl-5-(1-methylethenyl)-, (1.alpha.,2.alpha.,5.beta.)-