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menthene

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Identification
Molecular formula
C10H16
CAS number
99-82-1
IUPAC name
5-isopropyl-2-methyl-bicyclo[3.1.0]hex-2-ene
State
State

At room temperature, menthene is a liquid. Its volatility and pleasant aroma make it a component of various fragrances and essential oil blends.

Melting point (Celsius)
-90.00
Melting point (Kelvin)
183.15
Boiling point (Celsius)
169.00
Boiling point (Kelvin)
442.15
General information
Molecular weight
136.24g/mol
Molar mass
136.2380g/mol
Density
0.8190g/cm3
Appearence

Menthene is a colorless liquid with a strong and pleasant minty aroma. It is clear and transparent, resembling other essential oils in consistency.

Comment on solubility

Solubility of 5-isopropyl-2-methyl-bicyclo[3.1.0]hex-2-ene

The solubility of 5-isopropyl-2-methyl-bicyclo[3.1.0]hex-2-ene, a unique bicyclic compound, can be examined through various factors that influence its behavior in different solvents.

Key Considerations:

  • Polarity: The overall non-polar character of this compound suggests limited interaction with polar solvents, resulting in low solubility.
  • Hydrophobic Effects: Its hydrophobic nature indicates that it is more likely to dissolve in organic solvents such as hexane or heptane, rather than in water.
  • Temperature Dependency: The solubility can increase with temperature, as many non-polar compounds become more soluble in organic solvents when heated.

In summary, 5-isopropyl-2-methyl-bicyclo[3.1.0]hex-2-ene exhibits limited solubility in polar solvents and is best suited to dissolve in non-polar organic solvents. Practical applications and experimental procedures should take this into account to ensure effective use in various chemical contexts.

Interesting facts

Interesting Facts about 5-isopropyl-2-methyl-bicyclo[3.1.0]hex-2-ene

5-isopropyl-2-methyl-bicyclo[3.1.0]hex-2-ene is a fascinating compound that showcases the complexity and beauty of organic chemistry, specifically in the realm of bicyclic compounds. Here are some intriguing aspects:

  • Bicyclic Characteristics: As a bicyclic compound, this molecule features two interconnected rings, which can result in unique chemical behavior and reactivity compared to more linear structures. Bicyclic systems are often seen in natural products and pharmaceuticals.
  • Isomerism: The presence of substituents like isopropyl and methyl groups introduces interesting stereoisomerism possibilities. Studying these isomers can lead to insights into how small changes in structure can significantly affect a compound's chemical properties and interactions.
  • Applications: Compounds like 5-isopropyl-2-methyl-bicyclo[3.1.0]hex-2-ene can serve as important intermediates in the synthesis of more complex molecules. Understanding its reactivity plays a crucial role in synthesizing new drugs and materials.
  • Conformational Flexibility: The bicyclic structure allows for various conformations that may influence the compound's efficacy in biological systems. Chemists are often intrigued by how conformational changes can lead to different biochemical interactions.

In conclusion, 5-isopropyl-2-methyl-bicyclo[3.1.0]hex-2-ene exemplifies the intricacies of organic synthesis and structure-function relationships. Its unique configuration positions it as a candidate for further research and application in diverse fields, including medicinal chemistry and materials science.

Synonyms
ALPHA-THUJENE
2867-05-2
3-Thujene
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)-
THUJONE, (A + B)(SG)
2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene
.alpha.-Thujene
Thujone,(a + b)(sg)
2-Methyl-5-(1-methylethyl)-bicyclo(3.1.0)hex-2-ene
2-methyl-5-(1-methylethyl)-bicyclo[3.1.0]hex-2-ene
thujene (alpha-)
4-methyl-1-propan-2-ylbicyclo[3.1.0]hex-3-ene
Thujene, .alpha.-
5-Isopropyl-2-methylbicyclo[3.1.0]hex-2-ene
(-)-3-Thujene
(1R,5S)-thuj-2-ene
(1R)-(-)-thuj-3-ene
DTXSID20863038
DB-326055
NS00048720
EN300-7441739
5-Isopropyl-2-methylbicyclo[3.1.0]hex-2-ene #
Q27121796