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Menthofuran

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Identification
Molecular formula
C10H14O
CAS number
494-90-6
IUPAC name
1-methyl-4-(3-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane
State
State

At room temperature, menthofuran is in a liquid state.

Melting point (Celsius)
-18.00
Melting point (Kelvin)
255.15
Boiling point (Celsius)
228.00
Boiling point (Kelvin)
501.15
General information
Molecular weight
150.22g/mol
Molar mass
150.2210g/mol
Density
1.1070g/cm3
Appearence

Menthofuran is a colorless liquid with a fresh, slightly sweet odor. It is often extracted from peppermint and various other mint oils.

Comment on solubility

Solubility of 1-methyl-4-(3-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane

The solubility of 1-methyl-4-(3-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane can be quite intriguing due to its unique structural characteristics. Considering the compound's properties:

  • Polarity: The presence of the epoxide functional group can influence solubility; compounds containing polar functional groups tend to exhibit higher solubility in polar solvents.
  • Solvent Matching: This compound might be soluble in organic solvents such as ethanol, acetone, or dichloromethane, but less so in water due to its non-polar hydrocarbon structure.
  • Temperature Influence: Solubility is also impacted by temperature; typically, an increase in temperature can enhance the solubility of organic compounds in a solvent.
  • Concentration and Dilution: As with many compounds, high concentrations may lead to precipitation, while dilution in suitable solvents can increase its solubility.

In summary, while specific solubility data for this compound might not be readily available, understanding the factors that affect solubility—like polarity, solvent interactions, and temperature changes—is key in predicting how 1-methyl-4-(3-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane will behave in various environments.

Interesting facts

Interesting Facts about 1-methyl-4-(3-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane

1-methyl-4-(3-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane is a fascinating compound that belongs to a class of bicyclic organic compounds. Here are several intriguing aspects of this compound:

  • Structural Complexity: This compound features a bicyclic structure, characterized by its unique arrangement of carbon rings. The synthesis of bicyclic compounds often presents a challenge, making them of great interest in organic chemistry and materials science.
  • Functional Groups: The presence of an epoxide group, indicated by the methyloxirane component, adds to the reactivity of the molecule. Epoxides are known for their ability to undergo ring-opening reactions, which can lead to various chemical transformations.
  • Applications: Compounds such as 1-methyl-4-(3-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane are often investigated for their potential in pharmaceuticals and agrochemicals. Their complex structures may impart unique biological properties.
  • Synthetic Methodologies: The synthesis of this compound may involve advanced techniques such as asymmetric synthesis and cyclization reactions—topics of great relevance for chemists interested in creating specific stereoisomers and optimizing yields.
  • Research Potential: Ongoing studies on compounds like this one contribute to the expanding field of organics, particularly in areas such as drug discovery and materials development. Chemists are always on the lookout for compounds with novel properties that may lead to innovative applications.

In summary, 1-methyl-4-(3-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane stands as a testament to the complexity and beauty of organic chemistry. Its intriguing structure and reactivity profile offer a wealth of potential for exploration and innovation in scientific research.

Synonyms
1-methyl-4-(3-methyloxiran-2-yl)-7-oxabicyclo[4.1.0]heptane
DTXSID9042097
SCHEMBL1001233
CHEMBL3187590
YIEDFHHVUWKOEV-UHFFFAOYSA-N
Tox21_302214
CAS-96-08-2
NCGC00255956-01
NS00022909