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3-methylcatechol

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Identification
Molecular formula
C7H8O2
CAS number
488-17-5
IUPAC name
3-methylcyclohexa-3,5-diene-1,2-diol
State
State
At room temperature, 3-methylcatechol is a solid. It is typically stored in an airtight container to prevent oxidation.
Melting point (Celsius)
60.60
Melting point (Kelvin)
333.75
Boiling point (Celsius)
292.00
Boiling point (Kelvin)
565.15
General information
Molecular weight
126.14g/mol
Molar mass
126.1370g/mol
Density
1.2137g/cm3
Appearence

3-Methylcatechol appears as a white to off-white crystalline solid. It is prone to darkening upon exposure to air and light due to oxidation.

Comment on solubility

Solubility of 3-methylcyclohexa-3,5-diene-1,2-diol (C7H8O2)

The solubility of 3-methylcyclohexa-3,5-diene-1,2-diol is an intriguing topic that reflects the compound's unique structure and functional groups. This compound showcases both hydrocarbon and hydroxyl elements, which play critical roles in its dissolution behavior:

  • Polarity: The presence of the two hydroxyl (–OH) groups introduces polarity to the molecule, which enhances its ability to interact with polar solvents like water.
  • Hydrogen Bonding: These hydroxyl groups are capable of forming hydrogen bonds, thus increasing solubility in polar environments. This makes it more soluble in water compared to nonpolar solvents.
  • Hydrophobic Elements: Despite its polar features, the hydrophobic cyclohexene ring may limit solubility in high concentrations. This compound may demonstrate moderate solubility in organic solvents, owing to its hydrocarbon portion.

In summary, while 3-methylcyclohexa-3,5-diene-1,2-diol is likely to be more soluble in polar solvents than in nonpolar ones, the exact solubility will depend on the solvent's nature and temperature. "Understanding solubility is essential for practical applications ranging from pharmaceuticals to environmental science."

This makes studying the solubility profile an essential part of further investigations into this compound's behavior in various contexts.

Interesting facts

Interesting Facts about 3-methylcyclohexa-3,5-diene-1,2-diol

3-methylcyclohexa-3,5-diene-1,2-diol is a fascinating organic compound that presents a unique structure and exhibits a variety of interesting chemical properties. As a cyclic structure with multiple functional groups, it opens up various avenues for research and application.

Chemical Characteristics

  • Cyclic Structure: The presence of a cyclohexene ring contributes to the compound's stability and reactivity, which can be exploited in synthetic organic chemistry.
  • Diol Groups: The two hydroxyl (–OH) groups allow for hydrogen bonding, potentially leading to interesting interactions in biological contexts.
  • Conjugated Diene: With diene characteristics, the compound is prone to undergo reactions typical of alkenes, such as electrophilic addition reactions.

Potential Applications

Research shows that compounds like 3-methylcyclohexa-3,5-diene-1,2-diol can have potential applications in:

  • Synthesis: This compound can serve as an intermediate in the synthesis of more complex molecules.
  • Pharmaceuticals: The diol functionality often plays a crucial role in enhancing the solubility and bioavailability of drugs.
  • Material Science: The unique reactivity of this compound can be utilized in creating novel materials with specific properties.

Scientific Insight

As quoted by several researchers, “Understanding the subtleties of such organic compounds can lead to breakthroughs in both theoretical and applied chemistry.” Studying compounds like 3-methylcyclohexa-3,5-diene-1,2-diol not only enriches our knowledge of organic reactions but also inspires innovative approaches to chemical synthesis.

In conclusion, the intriguing features of 3-methylcyclohexa-3,5-diene-1,2-diol make it a subject of ongoing interest among chemists and a valuable compound in various scientific fields.

Synonyms
3-methylcyclohexa-3,5-diene-1,2-diol
SCHEMBL5048473
25506-13-2
DB-046719