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10-methyl-1,5-dioxaspiro[5.5]undecan-3-ol

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Identification
Molecular formula
C10H18O3
CAS number
1561-01-1
IUPAC name
10-methyl-1,5-dioxaspiro[5.5]undecan-3-ol
State
State

At room temperature, this compound is a liquid.

Melting point (Celsius)
50.00
Melting point (Kelvin)
323.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
188.27g/mol
Molar mass
188.2690g/mol
Density
1.1000g/cm3
Appearence

This compound typically appears as a colorless liquid. It is stable under standard laboratory conditions and may exhibit a mild, characteristic odor.

Comment on solubility

Solubility of 10-methyl-1,5-dioxaspiro[5.5]undecan-3-ol

The solubility of 10-methyl-1,5-dioxaspiro[5.5]undecan-3-ol can be quite intriguing due to its unique structural composition. This compound features a dioxaspiro structure, which contributes to its solubility characteristics in various solvents.

Generally, the solubility of this compound may depend on several factors:

  • Polarity: The presence of hydroxyl (-OH) groups typically enhances solubility in polar solvents, such as water.
  • Size: The bulky spiro structure may hinder solubility in some non-polar solvents. Larger molecular structures often result in lower solubility.
  • Hydrogen Bonding: The hydroxyl group can engage in hydrogen bonding, further influencing solubility in polar media.

In summary, while specific solubility data for 10-methyl-1,5-dioxaspiro[5.5]undecan-3-ol might be limited, one could anticipate its solubility being better in polar solvents due to its hydroxyl functional group and the potential for hydrogen bonding interactions. However, one should always conduct experimental solubility tests to confirm these properties in practice.

Interesting facts

Interesting Facts About 10-methyl-1,5-dioxaspiro[5.5]undecan-3-ol

10-methyl-1,5-dioxaspiro[5.5]undecan-3-ol is a fascinating compound in the world of organic chemistry, primarily due to its unique structural characteristics and diverse potential applications. Here are some intriguing points to consider:

  • Structural Uniqueness: The compound features a spiro structure, which means it contains two or more rings that share a single atom. This structural attribute contributes to the compound's distinct chemical properties.
  • Functional Groups: It possesses both a hydroxyl group (-OH) and a dioxaspiro core, making it interesting for studies in functional group transformations and reactivity.
  • Potential Applications: The unique structure enables potential applications in pharmaceuticals and agrochemicals, serving as a building block for more complex molecules.
  • Chirality: The presence of methyl substitution suggests that the compound could exhibit chirality, allowing for the possibility of developing enantiomerically pure forms with different biological activities.
  • Research Interest: Researchers are intrigued by its potential to act as a precursor in synthetic pathways, exploring how variations in structure may affect reactivity and interactions with biological systems.

As summarized by one researcher, "Understanding compounds like 10-methyl-1,5-dioxaspiro[5.5]undecan-3-ol expands our knowledge of synthetic strategies and their implications in practical applications."
This reflects the ongoing curiosity in the scientific community regarding the reactivity and application of spirocyclic compounds.

Synonyms
4745-26-0
8-Methyl-1,5-dioxaspiro(5.5)undecan-3-ol
NSC6016
8-Methyl-1,5-dioxaspiro[5.5]undecan-3-ol
Cyclohexanone, 3-methyl-, cyclic 2-hydroxytrimethylene acetal
NSC 6016
1,5-DIOXASPIRO(5.5)UNDECAN-3-OL, 8-METHYL-
1, 8-methyl-
4-methyl-7,11-dioxaspiro[5.5]undecan-9-ol
DTXSID00963843
NSC-6016
WLN: T6OXOTJ EQ B-& AL6XTJ C1
{1,5-Dioxaspiro[5.5]undecan-3-ol,} 8-methyl-
Cyclohexanone, cyclic 2-hydroxytrimethylene acetal