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Geranyl acetone

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Identification
Molecular formula
C14H24O2
CAS number
105-87-3
IUPAC name
1,1-diethoxy-3,7-dimethyl-octa-2,6-diene
State
State

Geranyl acetone is in a liquid state at room temperature.

Melting point (Celsius)
-67.00
Melting point (Kelvin)
206.15
Boiling point (Celsius)
274.50
Boiling point (Kelvin)
547.60
General information
Molecular weight
196.35g/mol
Molar mass
196.3240g/mol
Density
0.8600g/cm3
Appearence

Geranyl acetone typically appears as a colorless to pale yellow liquid. It has a pleasant, floral odor and is often used in the fragrance industry for its scent properties.

Comment on solubility

Solubility of 1,1-Diethoxy-3,7-dimethyl-octa-2,6-diene

The solubility of 1,1-diethoxy-3,7-dimethyl-octa-2,6-diene, often referred to for its complex structure, can vary significantly based on the solvent used. Understanding its solubility characteristics is crucial for applications in both industrial and laboratory settings. Here are some key points regarding its solubility:

  • Polar Solvents: Typically, compounds that contain multiple ethoxy groups exhibit some degree of solubility in polar solvents such as water due to hydrogen bonding, although the bulky nature of the diene structure may limit this effect.
  • Non-Polar Solvents: Its hydrophobic regions suggest that 1,1-diethoxy-3,7-dimethyl-octa-2,6-diene is likely to be more soluble in non-polar solvents like hexane or dichloromethane, making these solvents preferable for processes requiring dissolution.
  • Temperature Dependency: The solubility can also change with temperature; an increase in temperature typically enhances solubility, especially in non-polar solvents.
  • Overall Behavior: This compound may present a unique case where its solubility behavior is influenced by both its polar and non-polar characteristics, leading to a more intricate interaction with various solvents.

In conclusion, the solubility of 1,1-diethoxy-3,7-dimethyl-octa-2,6-diene is a balanced interplay between polar and non-polar characteristics. Thus, understanding the specific application and the choice of solvent is essential to optimize its solubility characteristics.

Interesting facts

Exploring 1,1-Diethoxy-3,7-Dimethyl-Octa-2,6-Diene

1,1-Diethoxy-3,7-dimethyl-octa-2,6-diene is a fascinating compound with unique characteristics that intrigue both chemists and enthusiasts of organic chemistry. Here are some interesting facts about this compound:

  • Structure and Bonding: This compound features a complex molecular structure that includes multiple functional groups. The presence of diethoxy groups enhances its reactivity and ability to participate in various chemical reactions.
  • Applications: 1,1-diethoxy-3,7-dimethyl-octa-2,6-diene finds its significance in organic synthesis and can serve as a building block for more complex molecules in pharmaceutical development.
  • Synthetic Pathways: The synthesis of this compound can involve various methods, including the use of diene metathesis or other catalytic reactions, making it an interesting subject for research in synthetic organic chemistry.
  • Reactivity: The diene component of this molecule suggests that it can undergo Diels-Alder reactions, making it valuable for creating cyclohexene derivatives, which are crucial in many organic synthesis pathways.
  • Potential Uses: Beyond pharmaceuticals, compounds like 1,1-diethoxy-3,7-dimethyl-octa-2,6-diene may have applications in materials science, such as in the development of new polymers or coatings due to their unique chemical properties.

In conclusion, the exploration of 1,1-diethoxy-3,7-dimethyl-octa-2,6-diene reveals a wealth of possibilities in the realms of organic synthesis and materials science. With ongoing research and innovation, the full potential of this compound is yet to be discovered!

Synonyms
(2E)-1,1-diethoxy-3,7-dimethylocta-2,6-diene
SCHEMBL119326
NTXGFKWLJFHGGJ-UHFFFAOYSA-N
DB-369954
NS00082453