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2-methyl-3-methylene-2-(4-methylpent-3-enyl)norbornane

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Identification
Molecular formula
C15H24
CAS number
489-53-4
IUPAC name
2-methyl-3-methylene-2-(4-methylpent-3-enyl)norbornane
State
State

At room temperature, this compound is in a liquid state.

Melting point (Celsius)
-97.20
Melting point (Kelvin)
175.95
Boiling point (Celsius)
271.00
Boiling point (Kelvin)
544.15
General information
Molecular weight
204.35g/mol
Molar mass
204.3510g/mol
Density
0.8478g/cm3
Appearence

2-Methyl-3-methylene-2-(4-methylpent-3-enyl)norbornane is typically a colorless liquid that may have a slight distinctive odor. It is composed of hydrocarbons and is generally hydrophobic, meaning it doesn't mix well with water.

Comment on solubility

Solubility of 2-methyl-3-methylene-2-(4-methylpent-3-enyl)norbornane

The solubility of 2-methyl-3-methylene-2-(4-methylpent-3-enyl)norbornane is an intriguing aspect of this compound, largely influenced by its molecular structure and the presence of hydrophobic alkyl groups. As a hydrocarbon compound, its solubility characteristics can be summarized as follows:

  • Non-polar Characteristics: Given its hydrocarbon nature, 2-methyl-3-methylene-2-(4-methylpent-3-enyl)norbornane exhibits low solubility in polar solvents such as water.
  • Solubility in Organic Solvents: This compound is expected to be soluble in non-polar organic solvents, including but not limited to:
    • Hexane
    • Ethyl acetate
    • Toluene
  • Thermodynamic Factors: The solubility is also affected by temperature and pressure; generally, greater temperatures increase the solubility of non-polar compounds in organic solvents.

In conclusion, while 2-methyl-3-methylene-2-(4-methylpent-3-enyl)norbornane shows limited solubility in polar environments, its compatibility with non-polar solvents offers a broader spectrum of application in organic chemistry. The interplay of its molecular structure and the solvent polarity plays a critical role in determining its solubility behavior.

Interesting facts

Interesting Facts about 2-methyl-3-methylene-2-(4-methylpent-3-enyl)norbornane

2-methyl-3-methylene-2-(4-methylpent-3-enyl)norbornane is a fascinating compound that showcases the beauty of organic chemistry. As a bicyclic hydrocarbon, it has unique structural characteristics that make it a subject of interest for chemists.

Key Highlights:

  • Complex Structure: This compound features a bicyclo[2.2.1]heptane core, which is a common skeleton in various natural products. The multiple substituents attached add to its complexity, demonstrating the creativity of molecular architecture.
  • Isomerism: The presence of several chiral centers allows for the existence of multiple stereoisomers, which can lead to different properties and biological activities, making it important in fields such as drug development.
  • Natural Occurrence: Compounds with similar structures often occur naturally in various plants and can have applications in perfumery and flavoring, emphasizing the connection between organic synthesis and nature.
  • Reactivity: The allylic side chains present in the molecule may be prone to various chemical reactions, such as electrophilic additions or eliminations, which can be harnessed in synthetic organic chemistry.
  • Research Potential: Its intricate design opens up possibilities for research into its physical and chemical properties, as well as potential applications in materials science and drug design.

This compound exemplifies the interplay between structure and function in organic chemistry. As we explore its properties and potential uses, the compound reminds us of the endless possibilities in the world of chemical science. As a quote goes, "Chemistry is the essence of life." This compound is a testament to that essence, inviting us to delve deeper into its mysteries.

Synonyms
Norbornane, 2-methyl-3-methylene-2-(4-methyl-3-pentenyl)-
b-Santalene
(-)-epi-beta-santalene
(+)-Epi-beta-Santalene
UNII-RG725C564C
2-Methyl-3-methylene-2-(4-methyl-3-pentenyl)bicyclo[2.2.1]heptane #
Bicyclo[2.2.1]heptane, 2-methyl-3-methylene-2-(4-methyl-3-pentenyl)-, (1S-endo)-