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Eucarvone

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Identification
Molecular formula
C15H24O
CAS number
119193-19-0
IUPAC name
4,12,12-trimethyl-9-methylene-5-oxatricyclo[8.2.0.04,6]dodecane
State
State
Eucarvone is typically in a liquid state at room temperature. It has a characteristic aroma, making it useful in perfumery and flavoring.
Melting point (Celsius)
25.00
Melting point (Kelvin)
298.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
208.32g/mol
Molar mass
208.3190g/mol
Density
0.9075g/cm3
Appearence

Eucarvone is a colorless liquid with a sweet and minty scent. It is commonly used in fragrance compositions for its pleasant odor.

Comment on solubility

Solubility of 4,12,12-trimethyl-9-methylene-5-oxatricyclo[8.2.0.04,6]dodecane

The compound 4,12,12-trimethyl-9-methylene-5-oxatricyclo[8.2.0.04,6]dodecane is an organic molecule featuring a complex structure, and its solubility can be influenced by various factors. Here are some key points regarding its solubility:

  • Nonpolar Characteristics: Due to its substantial hydrocarbon framework, this compound is likely to be nonpolar. Nonpolar compounds generally exhibit low solubility in polar solvents like water.
  • Solvent Compatibility: It is more likely to be soluble in nonpolar organic solvents such as hexane, benzene, or chloroform. This is due to the principle of "like dissolves like," where substances with similar polarity tend to dissolve well together.
  • Temperature Effects: The solubility may vary with temperature; typically, solubility of organic compounds increases with temperature. Therefore, conducting solubility tests at varying temperatures could yield more comprehensive insights.

In conclusion, the solubility characteristics of 4,12,12-trimethyl-9-methylene-5-oxatricyclo[8.2.0.04,6]dodecane suggest that while it may not dissolve well in polar solvents, exploring its solubility in nonpolar environments could provide valuable data. Always consider the specific conditions under which solubility is assessed for a more accurate understanding.

Interesting facts

Interesting Facts about 4,12,12-Trimethyl-9-methylene-5-oxatricyclo[8.2.0.04,6]dodecane

4,12,12-Trimethyl-9-methylene-5-oxatricyclo[8.2.0.04,6]dodecane is a fascinating compound that showcases the complexity and beauty of organic chemistry.

Chemical Structure and Characteristics

This compound is notable for its unique tricyclic structure, which results in intriguing properties and reactivity. Here are some key aspects:

  • Tricyclic Framework: The three interconnected rings contribute to the compound's stability and reactivity, making it an interesting subject for studying molecular interactions.
  • Functional Groups: The presence of oxatriene in the structure enhances its chemical versatility, allowing it to participate in various chemical reactions.
  • Isomers: Due to the multiple methyl groups and rings, this compound can exhibit several isomeric forms, each with distinct properties.

Applications and Implications

The potential applications of 4,12,12-trimethyl-9-methylene-5-oxatricyclo[8.2.0.04,6]dodecane are equally extraordinary:

  • Organic Synthesis: Its structure can serve as a valuable intermediate in organic synthesis, paving the way for more complex molecules.
  • Material Science: Due to its stable framework, it may find applications in the development of new materials with tailored properties.
  • Drug Design: The compound's unique structure can inspire the design of pharmaceuticals, providing a starting point for further modifications.

Conclusion

In summary, 4,12,12-trimethyl-9-methylene-5-oxatricyclo[8.2.0.04,6]dodecane is a prime example of the creativity found in organic chemistry. Its intricate structure and potential applications make it an exciting area of study for chemists and students alike. As one chemist wisely said, "Every molecule tells a story; we just need to listen."

Synonyms
4,12,12-trimethyl-9-methylene-5-oxatricyclo[8.2.0.04,6]dodecane
5-Oxatricyclo[8.2.0.04,6]dodecane, 4,12,12-trimethyl-9-methylene-
DTXSID50859585
5-Oxatricyclo(8.2.0.04,6)dodecane, 4,12,12-trimethyl-9-methylene-
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane
DTXCID60210426
241-609-3
Caryophyllene epoxide
13877-94-6
17627-43-9
Caryophyllene alpha-oxide
4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane
4,5-epoxy-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undecane
4,12,12-TRIMETHYL-9-METHYLIDENE-5-OXATRICYCLO[8.2.0.0?,?]DODECANE
4,5-Epoxy-4,11,11-trimethyl-8-methylenebicyclo(7.2.0)undecane
4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.0~4,6~]dodecane
b-Caryophyllene Epoxide
5-Oxatricyclo[8.2.0.0(4,6)-]dodecane, 4,12,12-trimethyl-9-methylene-, [1R-(1R*,4R*,6R*,10S*)]-
Isocaryophyllene, oxide
.beta.-Caryophyllene epoxide
(-)-.beta.-Caryophyllene oxide
5-Oxatricyclo[8.2.0.04,6]dodecane,4,12,12-trimethyl-9-methylene-
Caryophyllene oxyde
EINECS 237-642-8
EINECS 241-609-3
Caryophyllene a-oxide
SCHEMBL1532444
4,11,11-Trimethyl-8-methylene-5-oxatricyclo(8.2.0.0(4,6))dodecane, (1R,4R,6R,10S)-
CHEBI:156179
(-)-5-Oxatricyclo[8.2.0.0(4,6)]dodecane,4,12,12-trimethyl-9-methylene-, [1R-(1R*,4R*,6R*,10S*)]-
BBL034003
STL372857
AKOS024282622
(10S,1R,4R,6R)-4,12,12-trimethyl-9-methylene-5-oxatricyclo[8.2.0.0<4,6>]dodeca ne
SY011401
VS-12369
DB-060569
NS00012081
NS00101167
Q67879768
4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.0^{4,6}]dodecane