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Ambrettolide

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Identification
Molecular formula
C16H28O2
CAS number
106-02-5
IUPAC name
1-oxacycloheptadec-8-en-2-one
State
State

Ambrettolide is a liquid at room temperature, albeit with a slightly viscous, oily consistency.

Melting point (Celsius)
16.00
Melting point (Kelvin)
289.15
Boiling point (Celsius)
291.50
Boiling point (Kelvin)
564.70
General information
Molecular weight
268.43g/mol
Molar mass
268.4310g/mol
Density
0.9085g/cm3
Appearence

Ambrettolide is typically a colorless to pale yellow liquid. It is known for its musky scent, which is why it is often used in perfumery. It is slightly viscous, resembling oils or liquid wax in texture.

Comment on solubility

Solubility of 1-oxacycloheptadec-8-en-2-one

1-oxacycloheptadec-8-en-2-one, a compound with a unique structure, exhibits some intriguing solubility characteristics. Understanding its solubility can be pivotal for its applications in various fields. Here are some important points to note:

  • Solvent Interaction: This compound tends to show higher solubility in organic solvents compared to water due to its hydrophobic nature.
  • Hydrophilicity vs. Hydrophobicity: The presence of the oxacycloheptadec ring adds a degree of hydrophilicity; however, the overall long-chain hydrocarbon structure leans towards hydrophobicity.
  • Temperature Dependency: The solubility may vary significantly with temperature—generally, solubility increases with rising temperature in organic solvents.
  • Concentration Limits: At higher concentrations, the compound might reach saturation in certain solvents, leading to precipitation.

In summary, the solubility of 1-oxacycloheptadec-8-en-2-one is primarily influenced by its structural aspects and the solvent environment. Understanding these factors can help predict its behavior in chemical processes and formulations.

Interesting facts

Interesting Facts about 1-Oxacycloheptadec-8-en-2-one

1-Oxacycloheptadec-8-en-2-one, a member of the class of organic compounds known as lactones, presents an intriguing profile that captures the interest of chemists and researchers alike. This compound is notable for its unique ring structure and its functional groups that play vital roles in its chemical behavior and potential applications.

Key Features

  • Structural Diversity: The presence of a 7-membered ring coupled with a double bond offers a platform for diverse chemical reactivity.
  • Potential Biological Activity: Compounds of this class are often investigated for their biological properties, including antibacterial and antifungal activities. They may also serve as crucial intermediates in various synthesis processes.
  • Natural Occurrence: Many similar compounds are derived from natural products, which gives this compound a potential link to environmentally friendly chemistry.

Researchers value compounds like 1-oxacycloheptadec-8-en-2-one not only for their inherent chemical properties but also for their implications in industrial applications, including:

  • As starting materials in the synthesis of more complex molecules.
  • In the development of new materials with specific mechanical and electronic properties.
  • In medicinal chemistry, paving the way for innovative drug design.

In the Field of Research

As a chemist, one might explore the multifaceted roles of 1-oxacycloheptadec-8-en-2-one in various reactions, including:

  1. Nucleophilic Attacks: The electrophilic carbon in the ketone group can be targeted by nucleophiles, leading to a range of derivatives.
  2. Polymerization: The unsaturation in the ring may allow for polymer formation, which is of great interest in materials science.
  3. Functional Modification: The compound serves as a useful scaffold for the introduction of different functional groups, thus expanding its utility in synthetic chemistry.

In conclusion, 1-oxacycloheptadec-8-en-2-one stands as a testament to the complexity and beauty of organic chemistry. Its unique structure allows for a variety of functional applications, making it an important subject for ongoing research and development.

Synonyms
1-oxacycloheptadec-8-en-2-one
DTXSID30861762
Oxacycloheptadec-8-en-2-one
SpecPlus_000403
Spectrum3_001041
Spectrum4_001178
RefChem:1056168
KBioGR_001815
DivK1c_006499
SCHEMBL1539182
KBio1_001443
KBio3_001782
DTXCID40810645
NVIPUOMWGQAOIT-UHFFFAOYSA-N
DB-231605