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(1R,2S)-2-methylcyclohexanol

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Identification
Molecular formula
C7H14O
CAS number
7443-70-1
IUPAC name
(1R,2S)-2-methylcyclohexanol
State
State

At room temperature, it is a liquid.

Melting point (Celsius)
25.00
Melting point (Kelvin)
298.15
Boiling point (Celsius)
175.00
Boiling point (Kelvin)
448.15
General information
Molecular weight
114.19g/mol
Molar mass
114.1860g/mol
Density
0.9320g/cm3
Appearence

(1R,2S)-2-methylcyclohexanol is a colorless to pale yellow liquid. It may also appear as crystals depending on the temperature and the purity of the compound.

Comment on solubility

Solubility of (1R,2S)-2-methylcyclohexanol

(1R,2S)-2-methylcyclohexanol is an interesting compound as it showcases unique solubility properties. This compound, being an alcohol, exhibits moderate solubility in various solvents. Here are some key points regarding its solubility:

  • Water Solubility: Due to the presence of the hydroxyl group (-OH), (1R,2S)-2-methylcyclohexanol is likely to have some degree of solubility in water. However, the hydrophobic cyclohexane ring can limit this solubility.
  • Organic Solvents: This compound is expected to be significantly more soluble in organic solvents like ethanol, hexane, and acetone, because of the nonpolar character of the cyclohexane portion.
  • Temperature Influences: Solubility can also be influenced by temperature; increasing the temperature often improves the solubility of organic compounds in solvents.
  • Hydrophobic vs. Hydrophilic Balance: The balance between the hydrophobic (cyclohexane) and hydrophilic (alcohol) parts of the molecule plays a crucial role in its solubility profile.

In summary, while (1R,2S)-2-methylcyclohexanol displays moderate solubility in water due to its alcohol functional group, it tends to dissolve more readily in organic solvents, reflecting the impact of its molecular structure on solubility outcomes. Understanding this balance is essential in applications where solubility is a key factor.

Interesting facts

Interesting Facts about (1R,2S)-2-methylcyclohexanol

(1R,2S)-2-methylcyclohexanol is a fascinating compound known for its chiral nature, meaning it has non-superimposable mirror images. This characteristic plays a critical role in organic chemistry as it can lead to different properties and activities in biological systems. Here are some notable insights about this compound:

  • Chirality: The specific (1R,2S) configuration delivers unique interactions with other chiral molecules, impacting its pharmacological activity.
  • Applications: This compound is often utilized in the production of fragrances and flavoring agents due to its pleasant odor profile.
  • Solvent Properties: It can act as an effective intermediate in the synthesis of various organic compounds, showcasing its importance in the organic synthesis realm.
  • Research Significance: The study of (1R,2S)-2-methylcyclohexanol contributes to the understanding of stereoselective processes, a major theme in developing efficient synthesis methods in green chemistry.

In the realm of organic compounds, (1R,2S)-2-methylcyclohexanol represents the beautiful complexity of molecular structure and its implications. As one researcher aptly noted, "Understanding chirality is paramount to unlocking the potential of drug design and molecular interactions."

This compound, while relatively simple in structure, opens a myriad of discussions related to chirality and its impact in other fields such as environmental science and pharmacology, as scientists continue to explore the depths of its capabilities.

Synonyms
cis-2-Methylcyclohexanol
7443-70-1
Cyclohexanol, 2-methyl-, cis-
EINECS 231-187-9
NSC 100902
231-187-9
inchi=1/c7h14o/c1-6-4-2-3-5-7(6)8/h6-8h,2-5h2,1h
ndvwobybjyusmf-nkwvepmbsa-n
(1R,2S)-2-methylcyclohexan-1-ol
cis-2-Methylcyclohexan-1-ol
2-Methyl-cyclohexanol
cyclohexanol, 2-methyl-, (1R,2S)-
19043-02-8
SCHEMBL43021
BDBM36190
(+/-)-cis-2-methylcyclohexanol
DTXSID701032695
rel-(1R,2S)-2-Methylcyclohexanol
AKOS025295691
CS-0343026
D91322
InChI=1/C7H14O/c1-6-4-2-3-5-7(6)8/h6-8H,2-5H2,1H3/t6-,7+/m0/s