2,2-Diisobutyl-1,3-dioxolan-4-yl)methanol

Identification

Molecular formula

C₁₁H₂₂O₃

CAS number

100973-62-2

IUPAC name

(2,2-diisobutyl-1,3-dioxolan-4-yl)methanol

State

The compound is in a liquid state at room temperature, typically appearing as a clear, colorless liquid.

Melting point (Celsius)

-20.00

Melting point (Kelvin)

253.15

Boiling point (Celsius)

257.00

Boiling point (Kelvin)

530.15

General information

Molecular weight

188.29g/mol

Molar mass

188.2940g/mol

Density

0.9647g/cm³

Appearence

The compound is typically a colorless liquid that may exhibit a faint, characteristic odor. Its viscosity can vary depending on temperature, but it generally maintains a liquid state at standard room temperature and pressure.

Comment on solubility

Solubility of (2,2-diisobutyl-1,3-dioxolan-4-yl)methanol

The solubility of (2,2-diisobutyl-1,3-dioxolan-4-yl)methanol can be characterized by a few key features:

Polarity: This compound exhibits a moderate level of polarity due to the presence of hydroxyl (-OH) group and the dioxolane ring, which can interact with polar solvents.
Solvent Compatibility: It is likely that (2,2-diisobutyl-1,3-dioxolan-4-yl)methanol is soluble in polar organic solvents, such as ethanol and methanol, while showing limited solubility in non-polar solvents.
Temperature Dependence: Like many organic compounds, its solubility may increase with rising temperatures, which can lead to enhanced interactions with the solvent molecules.

In summary, while exact solubility data may vary, the compound's structure suggests it possesses a decent solubility profile in polar environments, making it an interesting candidate for various applications in organic synthesis and formulation.

Interesting facts

Interesting Facts about (2,2-Diisobutyl-1,3-dioxolan-4-yl)methanol

(2,2-Diisobutyl-1,3-dioxolan-4-yl)methanol is a fascinating compound that showcases the diversity of organic chemistry and its applications. Often used in various chemical syntheses, this compound has garnered attention for several reasons:

Structural Intrigue: The compound features a unique bicyclic dioxolane structure, which contributes to its reactivity and functional versatility.
Applications: It is often utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical and agrochemical industries.
Unique Properties: The presence of isobutyl groups imparts specific steric and electronic characteristics, influencing its behavior in chemical reactions.
Environmental Considerations: As with many compounds containing dioxolane rings, research is ongoing into the environmental impact and biodegradability of the derivatives derived from (2,2-diisobutyl-1,3-dioxolan-4-yl)methanol.

Additionally, the compound serves as a building block for more complex structures, highlighting the importance of understanding how small changes in molecular architecture can lead to significant variations in chemical behavior and application. As with many organic compounds, its synthesis often involves techniques such as electrophilic addition and nucleophilic substitution, showcasing the principles of reactivity in organic chemistry. Scientists continue to explore its potential uses, revealing deeper insights into its chemical properties and possible innovations.

In conclusion, (2,2-Diisobutyl-1,3-dioxolan-4-yl)methanol exemplifies the intricate relationships between structure, reactivity, and application in the vast field of organic chemistry. Its study offers a captivating blend of challenges and discoveries!

Synonyms

5694-81-5

2,2-Diisobutyl-1,3-dioxolane-4-methanol

BRN 0111389

1,3-DIOXOLANE-4-METHANOL, 2,2-DIISOBUTYL-

4-19-00-00684 (Beilstein Handbook Reference)

[2,2-bis(2-methylpropyl)-1,3-dioxolan-4-yl]methanol

SCHEMBL1677890

DTXSID60972390