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[2-methyl-2-(2-thienyl)-1,3-dioxolan-4-yl]methanol

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Identification
Molecular formula
C9H12O3S
CAS number
196224-57-6
IUPAC name
[2-methyl-2-(2-thienyl)-1,3-dioxolan-4-yl]methanol
State
State

At room temperature, the compound is a liquid. Its moderate boiling point and relatively low melting point contribute to its liquid state under normal atmospheric conditions.

Melting point (Celsius)
-12.00
Melting point (Kelvin)
261.15
Boiling point (Celsius)
212.00
Boiling point (Kelvin)
485.15
General information
Molecular weight
188.23g/mol
Molar mass
188.2290g/mol
Density
1.2120g/cm3
Appearence

The compound is a colorless to pale yellow liquid with a characteristic odor. It is often noted for its slightly sweet scent with a hint of earthy or woozy undertones, reminiscent of a thienyl group characteristic.

Comment on solubility

Solubility of [2-methyl-2-(2-thienyl)-1,3-dioxolan-4-yl]methanol

The solubility of the compound [2-methyl-2-(2-thienyl)-1,3-dioxolan-4-yl]methanol can be influenced by various factors due to its unique structure. Understanding its solubility behavior is crucial for applications and reactions involving this compound.

Factors Influencing Solubility

  • Polarity: The presence of hydroxyl (-OH) groups generally increases solubility in polar solvents like water.
  • Functional Groups: The dioxolane ring and thienyl substituent may impact interactions with solvents.
  • Temperature: Solubility often increases with temperature, particularly in organic solvents.

Some points to consider about its solubility are:

  1. Hydrogen Bonding: The -OH group can form hydrogen bonds, enhancing solubility in polar solvents.
  2. Solvent Compatibility: Likely soluble in organic solvents like ethanol and dimethyl sulfoxide (DMSO), but might have lower solubility in non-polar solvents.
  3. Concentration: At higher concentrations, the solubility limit may be reached, affecting its behavior in solutions.

In conclusion, the solubility of [2-methyl-2-(2-thienyl)-1,3-dioxolan-4-yl]methanol is an intricate balance of structural characteristics and environmental factors. Effective experimentation can reveal more detailed solubility parameters.

Interesting facts

Interesting Facts About [2-methyl-2-(2-thienyl)-1,3-dioxolan-4-yl]methanol

[2-methyl-2-(2-thienyl)-1,3-dioxolan-4-yl]methanol is a fascinating compound that showcases the intriguing interplay between organic chemistry and functional group diversity. Its structure features a dioxolane ring, a lesser-known yet significant motif in organic molecules, which contributes to its unique chemical properties.

Structural Features

This compound is characterized by:

  • Methyl Substitution: The presence of a methyl group enhances stability and may influence reactivity.
  • Thienyl Group: The thienyl moiety introduces aromaticity and electrochemical behavior, which could play a role in various applications.
  • Dioxolane Framework: This five-membered ring is often associated with a variety of chemical reactions, making it a building block for more complex architectures.

Applications and Significance

The compound can potentially serve as a precursor or an intermediate in the synthesis of:

  • Pharmaceuticals: Compounds containing dioxolanes are studied for their biological activities, including anticancer and antimicrobial properties.
  • Materials Science: The unique structural features might enable its incorporation into polymers or other advanced materials.
  • Organic Synthesis: The compound can be utilized in various synthetic pathways due to its reactive functional groups.

Research and Development

Current studies on compounds like [2-methyl-2-(2-thienyl)-1,3-dioxolan-4-yl]methanol highlight the importance of:

  • Green Chemistry: Investigations into more sustainable production methods.
  • Mechanistic Insights: Understanding the reactivity of the dioxolane structure under different conditions.
  • Structurally Diverse Libraries: Expanding the library of compounds for drug discovery and materials research.

In conclusion, [2-methyl-2-(2-thienyl)-1,3-dioxolan-4-yl]methanol exemplifies the breadth of organic chemical research, revealing both its complexity and potential. It invites further exploration and development in various scientific fields, reflecting the intricate nature of modern chemistry.

Synonyms
4361-62-0
2-Methyl-2-(2-thienyl)-1,3-dioxolane-4-methanol
1,3-DIOXOLANE-4-METHANOL, 2-METHYL-2-(2-THIENYL)-
(2-methyl-2-thiophen-2-yl-1,3-dioxolan-4-yl)methanol
DTXSID10963091
[2-METHYL-2-(THIOPHEN-2-YL)-1,3-DIOXOLAN-4-YL]METHANOL