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(2,5-dimethyl-1-vinyl-hex-4-enyl) 3-methylbutanoate

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Identification
Molecular formula
C16H30O2
CAS number
: 68917-54-2
IUPAC name
(2,5-dimethyl-1-vinyl-hex-4-enyl) 3-methylbutanoate
State
State
The compound is a liquid at room temperature, exhibiting a moderate viscosity.
Melting point (Celsius)
-55.00
Melting point (Kelvin)
218.15
Boiling point (Celsius)
260.40
Boiling point (Kelvin)
533.60
General information
Molecular weight
254.40g/mol
Molar mass
254.4030g/mol
Density
0.8290g/cm3
Appearence

(2,5-dimethyl-1-vinyl-hex-4-enyl) 3-methylbutanoate is typically a colorless liquid, though it might have a slight yellowish tint. It has a noticeable fruity aroma.

Comment on solubility

Solubility of (2,5-dimethyl-1-vinyl-hex-4-enyl) 3-methylbutanoate

The solubility of the compound (2,5-dimethyl-1-vinyl-hex-4-enyl) 3-methylbutanoate can be influenced by various factors, including its molecular structure and the surrounding environment. This compound, with its intricate arrangement of functional groups, presents certain characteristics affecting its solubility:

  • Polarity: The presence of ester functional groups typically increases polarity, which can enhance solubility in polar solvents like water.
  • Hydrocarbon Chain: The long hydrocarbon chain in this compound can lead to hydrophobic interactions, making it less soluble in water but more soluble in non-polar organic solvents such as hexane or ether.
  • Temperature: As with many organic compounds, solubility can vary with temperature. Higher temperatures may increase solubility in certain solvents.
  • Concentration of Solvents: Concentration of the solute and solvent can determine the degree of solubility, impacting how much of the compound can dissolve in a particular solvent.

In summary, while (2,5-dimethyl-1-vinyl-hex-4-enyl) 3-methylbutanoate is likely to exhibit limited solubility in water, it may find greater solubility in organic solvents, echoing the adage that "like dissolves like." Understanding these solubility characteristics is essential for practical applications such as synthesis and formulation in scientific research and industry.

Interesting facts

Interesting Facts about (2,5-Dimethyl-1-vinyl-hex-4-enyl) 3-methylbutanoate

(2,5-dimethyl-1-vinyl-hex-4-enyl) 3-methylbutanoate is a compound that showcases the fascinating interplay of organic chemistry and natural fragrance. Here are some intriguing aspects of this compound:

  • Flavors & Aromas: Compounds like (2,5-dimethyl-1-vinyl-hex-4-enyl) 3-methylbutanoate are often utilized in the fragrance and flavor industry for their pleasant aromas. They can contribute to fruity or floral notes in various products.
  • Applications: This compound can be found in perfumes, food flavorings, and even cosmetic formulations. Its unique structure allows it to bind taste and scent receptors, making it an essential ingredient in the creation of specific olfactory profiles.
  • Synthetic Pathways: The synthesis of (2,5-dimethyl-1-vinyl-hex-4-enyl) 3-methylbutanoate can involve various organic reactions, such as esterification and alkylation. Understanding these pathways is crucial for chemists working in industries that require aromatic compounds.
  • Structural Intricacies: The presence of multiple methyl groups and a vinyl group in its structure contributes to its reactivity and potential transformations in different chemical environments.
  • Research and Development: Ongoing research in organic chemistry may lead to the development of more efficient synthetic routes to produce compounds like (2,5-dimethyl-1-vinyl-hex-4-enyl) 3-methylbutanoate, enhancing its availability for commercial applications.

As scientists and students explore the world of this compound, they uncover not only its practical uses but also the underlying principles of organic chemistry that govern its behavior in various applications.

Synonyms
ISOVALERIC ACID (4,7-DIMETHYL-1,6-OCTADIEN-3-YL) ESTER
SCHEMBL1532663