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Bicyclo[3.2.1]octan-2-ol

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Identification
Molecular formula
C8H14O
CAS number
14993-85-0
IUPAC name
bicyclo[3.2.1]octan-2-ol
State
State

At room temperature, bicyclo[3.2.1]octan-2-ol can be found as a solid or liquid depending on the purity and environmental conditions.

Melting point (Celsius)
55.00
Melting point (Kelvin)
328.15
Boiling point (Celsius)
215.00
Boiling point (Kelvin)
488.15
General information
Molecular weight
126.20g/mol
Molar mass
126.1960g/mol
Density
1.0300g/cm3
Appearence

Bicyclo[3.2.1]octan-2-ol appears as a colorless liquid or solid depending on the temperature, with a characteristic camphor-like odor. Its appearance can vary between a crystalline solid or a clear liquid.

Comment on solubility

Solubility of Bicyclo[3.2.1]octan-2-ol

Bicyclo[3.2.1]octan-2-ol is an intriguing compound when it comes to solubility. Its unique bicyclic structure contributes to its solubility properties, which can vary significantly depending on the solvent used. Here are some key points regarding its solubility:

  • Polar solvents: Bicyclo[3.2.1]octan-2-ol is likely to have higher solubility in polar solvents due to the presence of the hydroxyl group (-OH)
  • Non-polar solvents: Its solubility in non-polar solvents may be limited due to the hydrophilic nature of the hydroxyl group which prefers interaction with polar environments.
  • Temperature factors: Generally, solubility can also be affected by temperature; as the temperature increases, solubility in most solvents tends to rise.

In summary, the solubility of bicyclo[3.2.1]octan-2-ol will largely depend on the solvent's polarity, and it exemplifies how molecular structure intricately influences solubility behavior. As the study of such compounds continues, understanding their solubility trends can lead to valuable applications in various chemical processes.

Interesting facts

Interesting Facts About Bicyclo[3.2.1]octan-2-ol

Bicyclo[3.2.1]octan-2-ol, commonly referred to as a bicyclic compound, offers a unique perspective in the world of organic chemistry. Here are some intriguing aspects of this fascinating compound:

  • Structural Uniqueness: This compound features a bicyclic structure that consists of two interconnected rings. This configuration leads to significant strain in the rings, which can influence its reactivity and properties.
  • Natural Occurrence: Certain compounds related to bicyclo[3.2.1]octan-2-ol can be found in nature, contributing to the diversity of organic molecules present in various biological systems.
  • Synthetic Applications: Bicyclic compounds like bicyclo[3.2.1]octan-2-ol are often of interest in synthetic organic chemistry as intermediates in the synthesis of larger, more complex molecules. They serve as key building blocks in the production of agrochemicals, pharmaceuticals, and fine chemicals.
  • Research Relevance: This compound has garnered attention in the field of drug design due to its ability to act as a scaffold for creating bioactive molecules. Its unique spatial arrangement offers opportunities for enhancing molecule-target interactions.
  • Role in Stereochemistry: The presence of stereocenters in bicyclo[3.2.1]octan-2-ol makes it an important subject of study in stereochemistry, challenging chemists to explore its isomers and their distinct chemical behaviors.

In summary, bicyclo[3.2.1]octan-2-ol serves as a prime example of the interplay between structure and function in organic chemistry. Its distinctive features and applications underscore the compound's significance in both academic research and industrial applications.

Synonyms
Bicyclo[3.2.1]octan-2-ol
1965-38-4
5602-48-2
rac-(1R,2R,5R)-Bicyclo[3.2.1]octan-2-ol, exo
NSC408795
EXOBICYCLO(3.2.1)-2-OCTANOL
NCIOpen2_003578
SCHEMBL2884397
DTXSID50941414
PVDVHTXERCKKSW-UHFFFAOYSA-N
BAA96538
NSC-408795
EN300-701176