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Dihydroactinidiolide

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Identification
Molecular formula
C10H16O2
CAS number
17092-92-1
IUPAC name
4,6,6-trimethyltetrahydropyran-2-one
State
State

At room temperature, dihydroactinidiolide is in a liquid state.

Melting point (Celsius)
53.00
Melting point (Kelvin)
326.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
168.24g/mol
Molar mass
168.2370g/mol
Density
1.0220g/cm3
Appearence

Dihydroactinidiolide is a colorless to pale yellow liquid with a weak, sweet, and tea-like odor. It is often found in nature and in various plants.

Comment on solubility

Solubility of 4,6,6-trimethyltetrahydropyran-2-one

4,6,6-trimethyltetrahydropyran-2-one, a cyclic ketone, exhibits intriguing solubility characteristics that can influence its applications and reactivity. Understanding its solubility can be summarized as follows:

  • Polarity: The structure of this compound suggests a moderate polarity due to the presence of both the cyclic ether and the ketone functional group.
  • Solvents: It is generally more soluble in organic solvents such as ethanol, methanol, and other similar polar protic solvents, while displaying lower solubility in water.
  • Temperature Influence: Like many organic compounds, solubility can significantly increase with temperature; thus, heating the solvent may enhance the dissolution process.

In summary, while 4,6,6-trimethyltetrahydropyran-2-one is not highly soluble in water, it finds better solubility in various organic solvents. Proper solvation conditions and careful selection of solvents can maximize its effective use in chemical processes.

Interesting facts

Interesting Facts about 4,6,6-trimethyltetrahydropyran-2-one

4,6,6-trimethyltetrahydropyran-2-one is a fascinating compound that belongs to the class of cyclic ketones, notably characterized by the presence of a tetrahydropyran ring. This compound has garnered attention in various fields for its potential applications and unique structural attributes.

Key Features

  • Structural Diversity: The presence of three methyl groups at the 4, 6, and 6 positions of the tetrahydropyran ring contributes to the compound's unique stereochemistry, impacting its reactivity and physical properties.
  • Natural Products: Compounds similar to 4,6,6-trimethyltetrahydropyran-2-one often occur in nature, particularly in plants, presenting opportunities for extraction and study.
  • Potential Applications: This compound and its derivatives have been researched for their roles as intermediates in organic synthesis, making them valuable in the production of pharmaceuticals and other fine chemicals.
  • Flavors and Fragrances: Structurally related cyclic compounds are widely used in flavours and fragrances, hinting at the compound’s potential use in the food and cosmetic industries.

In the words of chemist Robert H. Grubbs, “The beauty of chemistry resides in its ability to create a seemingly endless variety of compounds.” 4,6,6-trimethyltetrahydropyran-2-one vividly exemplifies this idea, showcasing how small modifications in structure can lead to significant variations in property and utility.

This compound also serves as a teaching model in organic chemistry, illustrating key concepts like chirality, the role of functional groups, and the synthesis of complex molecules. With continued research, 4,6,6-trimethyltetrahydropyran-2-one holds promise for innovative advancements in multiple scientific domains.

Synonyms
20628-36-8
Tetrahydro-4,6,6-trimethyl-2H-pyran-2-one
EINECS 243-927-8
2H-Pyran-2-one, tetrahydro-4,6,6-trimethyl-
NSC 134776
243-927-8
RefChem:188624
4,6,6-trimethyloxan-2-one
NSC134776
SCHEMBL10431444
DTXSID501272827
2H-Pyran-2-one,6,6-trimethyl-
NSC-134776
NS00051450
4,6,6-Trimethyltetrahydro-2H-pyran-2-one #