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Coniferyl alcohol

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Identification
Molecular formula
C10H12O3
CAS number
458-35-5
IUPAC name
4-(3-hydroxyprop-1-enyl)-2-methoxy-phenol
State
State

Solid at room temperature, commonly found as a white to light yellow crystalline powder.

Melting point (Celsius)
73.00
Melting point (Kelvin)
346.00
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.00
General information
Molecular weight
180.20g/mol
Molar mass
180.1960g/mol
Density
1.0861g/cm3
Appearence

Coniferyl alcohol is a light yellow to white crystalline solid. It possesses a slight phenolic odor that is characteristic of many aromatic alcohols.

Comment on solubility

Solubility of 4-(3-hydroxyprop-1-enyl)-2-methoxy-phenol

The compound 4-(3-hydroxyprop-1-enyl)-2-methoxy-phenol exhibits interesting solubility characteristics. This organic compound, which contains both hydrophilic and hydrophobic functional groups, leads to a dynamic solubility profile.

Key Factors Influencing Solubility:

  • Presence of Hydroxy Groups: The hydroxyl (-OH) group enhances hydrophilicity, allowing the compound to dissolve better in polar solvents like water.
  • Methoxy Substitution: The methoxy (-OCH3) group contributes to lipophilicity, which can favor solubility in organic solvents such as ethanol or acetone.
  • Structural Configuration: The overall molecular structure impacts how the compound interacts with solvents, particularly in terms of steric hindrance and molecular flexibility.

In general: This compound is likely to show moderate solubility in water, while exhibiting higher solubility in organic solvents. It’s important to note that the specific solubility can be affected by temperature and the presence of other solutes.

As a guideline, solubility can vary, which makes empirical testing crucial for precise applications. Remember, "like dissolves like," so understanding the solvent's nature will lead to better predictions of the compound's solubility!

Interesting facts

Interesting Facts about 4-(3-hydroxyprop-1-enyl)-2-methoxy-phenol

4-(3-hydroxyprop-1-enyl)-2-methoxy-phenol, often recognized in the field of chemistry for its unique structure, presents a fascinating array of characteristics and potential applications:

  • Natural Occurrence: This compound is related to various natural phenolic compounds, suggesting its presence in plants and their extracts, which have been utilized for medicinal purposes.
  • Antioxidant Properties: It has been studied for its ability to scavenge free radicals, which can help protect cells from oxidative stress—an important factor in many chronic diseases.
  • Flavor and Aroma: Compounds related to this structure can contribute to the flavor and aroma profiles of certain foods, making them of interest to the food science community.
  • Biological Activities: Research indicates potential biological activities, including anti-inflammatory and antimicrobial effects, which open avenues for drug development.
  • Synthesis: The synthetic routes to create this compound often involve straightforward procedures, making it accessible for laboratory studies and research applications.

As a result of these diverse properties, 4-(3-hydroxyprop-1-enyl)-2-methoxy-phenol is more than just a chemical entity; it embodies the intricate relationship between structure and function in organic compounds.

As one scientific review eloquently described it, "the beauty of chemical compounds lies in their ability to influence health and flavor through mere adjustments in their molecular architecture." Thus, the exploration of this compound not only enhances our understanding of chemistry but also our connection to everyday life.

Synonyms
Phenol, 4-(3-hydroxy-1-propenyl)-2-methoxy-
4-(3-Hydroxyprop-1-en-1yl)-2-methoxyphenol
DTXSID9060029
(E/Z)-Coniferol; 4-Hydroxy-3-methoxycinnamyl alcohol (cis/trans mixture)
Oprea1_201369
AKOS028108458
DB-051336
3-(4-hydroxy-3-methoxyphenyl)-prop-2-enol