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1-methylcyclohex-2-en-1-ol

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Identification
Molecular formula
C7H12O
CAS number
1193-47-1
IUPAC name
1-methylcyclohex-2-en-1-ol
State
State

At room temperature, 1-methylcyclohex-2-en-1-ol is found in a liquid state.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
196.00
Boiling point (Kelvin)
469.15
General information
Molecular weight
112.17g/mol
Molar mass
112.1720g/mol
Density
0.9155g/cm3
Appearence

1-Methylcyclohex-2-en-1-ol typically appears as a colorless to pale yellow liquid. It has a characteristic, faint odor.

Comment on solubility

Solubility of 1-methylcyclohex-2-en-1-ol

1-methylcyclohex-2-en-1-ol, with its unique structure characterized by both cyclic and unsaturated features, displays interesting solubility characteristics:

  • Polar vs. Non-Polar Solvents: Its hydroxyl (-OH) group imparts some degree of polarity, making it soluble in polar solvents such as water and alcohols. However, the hydrophobic character of the cyclohexene framework may limit its solubility in highly polar environments.
  • Cosolvent Systems: In practice, mixing 1-methylcyclohex-2-en-1-ol with non-polar solvents like hexane can lead to varying degrees of solubility depending on the specific conditions and concentrations.
  • Saturation Points: It is essential to note that the solubility can reach saturation points, after which no further dissolution occurs, leading to precipitation in cases of higher concentrations.

In summary, the solubility of 1-methylcyclohex-2-en-1-ol can be best understood through the lens of its functional groups and molecular characteristics. As such, “the key is to pair it with the right solvent” to enhance its solubility properties effectively!

Interesting facts

Interesting Facts about 1-methylcyclohex-2-en-1-ol

1-methylcyclohex-2-en-1-ol, also known as a type of cyclohexene derivative, is a fascinating compound with several intriguing characteristics that make it an interesting topic of study:

  • Structural Unique: This compound features a cyclohexene ring with a double bond and a hydroxyl (–OH) group incorporated in its structure, which contributes to its reactivity and potential applications in organic synthesis.
  • Natural Occurrence: Compounds like 1-methylcyclohex-2-en-1-ol can be found in various essential oils and plant extracts, hinting at its role in natural chemistry and potential uses in flavor and fragrance industries.
  • Reactivity: As an allylic alcohol, this compound offers interesting pathways for chemical reactivity, including nucleophilic substitution and various addition reactions. This makes it a valuable intermediate in organic synthesis.
  • Hydroxyl Influence: The presence of the hydroxyl group not only lends itself to hydrogen bonding but also increases its polarity, influencing its interactions with other compounds and solvents.
  • Applications: Due to its structural features, 1-methylcyclohex-2-en-1-ol may have potential applications in the development of agrochemicals, pharmaceuticals, and as a building block in the synthesis of more complex molecules.

In summary, the unique structure and properties of 1-methylcyclohex-2-en-1-ol make it a compound of great interest in both academic research and industrial applications. As chemistry continues to advance, compounds like these are at the forefront of innovation in various scientific fields.

Synonyms
1-METHYL-2-CYCLOHEXEN-1-OL
23758-27-2
RefChem:1055758
1-methylcyclohex-2-en-1-ol
2-Cyclohexen-1-ol, 1-methyl-
SCHEMBL2573506
SCHEMBL11037585
1-Methyl-2-cyclohexen-1-ol #
DTXSID10946541
LVUQVFWOWNKFRL-UHFFFAOYSA-N
AKOS026727301
EN300-138283
Z1691624687