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(1R)-3-methylcyclohexanol

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Identification
Molecular formula
C7H14O
CAS number
5912-85-2
IUPAC name
(1R)-3-methylcyclohexanol
State
State

This compound is a liquid at room temperature.

Melting point (Celsius)
-15.00
Melting point (Kelvin)
258.15
Boiling point (Celsius)
176.90
Boiling point (Kelvin)
450.05
General information
Molecular weight
114.19g/mol
Molar mass
114.1860g/mol
Density
0.9254g/cm3
Appearence

(1R)-3-methylcyclohexanol is a colorless liquid with a camphor-like odor. It is typically clear and used in various chemical syntheses due to its chiral properties.

Comment on solubility

Solubility of (1R)-3-methylcyclohexanol

The solubility of (1R)-3-methylcyclohexanol can be described through a few critical aspects:

  • Polarity: This compound is relatively polar due to the presence of the hydroxyl group (-OH), which tends to increase solubility in polar solvents.
  • Hydrophilic vs. Hydrophobic: The cyclohexanol structure introduces a hydrophobic character due to its carbon ring, which can counterbalance the polar nature of the hydroxyl group.
  • Solvent Interaction: It has higher solubility in organic solvents such as ethanol and acetone compared to water, due to its hydrophobic characteristics.

In summary, while (1R)-3-methylcyclohexanol exhibits some solubility in polar solvents due to its -OH group, its overall solubility profile is influenced by the balance of its polar and nonpolar regions. It is essential to consider the environmental conditions, as factors such as temperature can also play a significant role in the solubility characteristics of this compound.

Interesting facts

Interesting Facts about (1R)-3-Methylcyclohexanol

(1R)-3-Methylcyclohexanol is an intriguing compound within the family of alcohols, known for its unique structural properties and applications in various fields. Here are some captivating insights into this chemical:

  • Structural Isomerism: This compound exhibits fascinating structural isomerism, which means that despite having the same molecular formula as other compounds, its arrangement of atoms is distinct. This characteristic can lead to varying physical and chemical properties, making (1R)-3-methylcyclohexanol interesting for studies in stereochemistry.
  • Natural Occurrence: One of the remarkable features of this alcohol is its presence in natural sources. It can be found in certain essential oils and contributes to the aroma and flavor profiles of some plants, which makes it a subject of interest in the fields of perfumery and flavor chemistry.
  • Chiral Center: The designation of (1R) indicates that this compound has a chiral center, making it optically active. Chirality is critical in pharmaceuticals, as the different enantiomers of a compound can have different biological effects, underscoring the importance of proper enantiomer selection in drug development.
  • Reactivity and Derivatives: (1R)-3-Methylcyclohexanol can undergo various chemical reactions such as oxidation and esterification, leading to the creation of derivatives that may exhibit unique properties. Such transformations can be vital in synthetic chemistry, allowing for the development of new materials and compounds.
  • Application in Organic Synthesis: The compound is often utilized as a building block in organic synthesis, contributing to the production of more complex chemical entities. Its versatility in chemical reactions aids in expanding the toolkit of organic chemists.

In conclusion, (1R)-3-Methylcyclohexanol holds a noteworthy position in both academic research and industrial applications, serving as a prime example of how the simple structures of alcohols can lead to complex and varied implications in science and technology.

Synonyms
trans-3-Methylcyclohexanol
7443-55-2
Cyclohexanol, 3-methyl-, trans-
SCHEMBL14042004
DTXSID001032694