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[4-(4-bromo-3,3-dimethyl-cyclohexyl)-2,3-dioxabicyclo[2.2.2]oct-5-en-1-yl]methanol

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Identification
Molecular formula
C13H19BrO3
CAS number
705-74-8
IUPAC name
[4-(4-bromo-3,3-dimethyl-cyclohexyl)-2,3-dioxabicyclo[2.2.2]oct-5-en-1-yl]methanol
State
State

The compound is a solid at room temperature. The specific combination of rings and substituents in its structure contribute to its solid-state stability. Its physical state allows it to be conveniently handled and measured in laboratory settings.

Melting point (Celsius)
130.00
Melting point (Kelvin)
403.15
Boiling point (Celsius)
395.00
Boiling point (Kelvin)
668.15
General information
Molecular weight
292.16g/mol
Molar mass
292.1640g/mol
Density
1.3400g/cm3
Appearence

This compound typically appears as a white crystalline solid. Its structure contains a cyclohexyl group with a bromine atom and a bicyclic dioxabicyclo compound, which gives it a characteristic shape and rigidity. The presence of the hydroxyl group contributes to its potential chemical reactivity.

Comment on solubility

Solubility of [4-(4-bromo-3,3-dimethyl-cyclohexyl)-2,3-dioxabicyclo[2.2.2]oct-5-en-1-yl]methanol

The solubility of a compound often reveals critical insights into its chemical properties and potential applications. For the compound [4-(4-bromo-3,3-dimethyl-cyclohexyl)-2,3-dioxabicyclo[2.2.2]oct-5-en-1-yl]methanol with a chemical formula of C13H19BrO3, we can examine several aspects affecting its solubility:

  • Polarity: The presence of the –OH (hydroxyl) group suggests that the compound can form hydrogen bonds, potentially increasing its solubility in polar solvents such as water.
  • Hydrophobic characteristics: The bulky cyclohexyl groups and bromine atom may reduce solubility in polar solvents while offering better solubility in non-polar solvents like oils or organic solvents.
  • Structural configuration: The bicyclic structure could impose steric hindrance, possibly affecting molecular interactions and altering solubility behavior in various solvents.

In general, compounds with similar structures may display varied solubility depending on the solvent type. As a rule of thumb, "like dissolves like" holds true. In this case, potential solubility in:

  • Water: Low to moderate, influenced by the hydrophilic nature of the alcohol group.
  • Organic solvents: Likely higher due to the hydrophobic portions of the molecule.

Therefore, the solubility of [4-(4-bromo-3,3-dimethyl-cyclohexyl)-2,3-dioxabicyclo[2.2.2]oct-5-en-1-yl]methanol remains complex and multifaceted, revealing the interplay between its structural components and their interactive capabilities with solvents.

Interesting facts

Interesting Facts about [4-(4-bromo-3,3-dimethyl-cyclohexyl)-2,3-dioxabicyclo[2.2.2]oct-5-en-1-yl]methanol

This fascinating compound is a member of the bicyclic family of organic molecules, showcasing the intricate complexity that can arise within chemical structures. Its unique attributes lead to various intriguing applications and research avenues:

  • Structural Diversity: The compound features a bicyclo[2.2.2]octene framework, which is notable for its ability to create unique stereochemical arrangements. Research in this area can yield insights into conformational preferences and the impact of stereochemistry on reactivity.
  • Potential Biological Activity: Compounds similar to this one have been investigated for their biological properties. The presence of a bromine atom and the complex cyclohexane structure suggest potential interactions with biological targets, making it a candidate for pharmaceutical research.
  • Applications in Material Science: The dual hydroxyl groups in the structure can facilitate diverse interactions, making this compound a subject of interest for development in material science, particularly in creating novel polymers and coatings.
  • Environmental Relevance: The use of bromine in organic synthesis highlights potential implications for environmental science, as such compounds often undergo unique pathways within ecological systems, allowing for studies on their degradation and impact.

As a scientist or a chemistry student, exploring compounds with such intricate architectures provides a thrilling journey into the world of organic synthesis and application. The complexity of this compound could inspire future innovations in medicinal chemistry and materials engineering, presenting a *rich field of study* that intertwines various disciplines within science.

Synonyms
Majapolene A
NSC692207
[4-(4-bromo-3,3-dimethylcyclohexyl)-2,3-dioxabicyclo[2.2.2]oct-5-en-1-yl]methanol
(4-((1S,4S)-4-bromo-3,3-dimethylcyclohexyl)-2,3-dioxabicyclo(2.2.2)oct-5-en-1-yl)methanol
[4-[(1S,4S)-4-bromo-3,3-dimethylcyclohexyl]-2,3-dioxabicyclo[2.2.2]oct-5-en-1-yl]methanol
CHEMBL450193
NSC-692207
1092795-43-1