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Prenyl phenol

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Identification
Molecular formula
C11H14O
CAS number
1442-72-6
IUPAC name
4-(3-methylbut-2-enyl)phenol
State
State

At room temperature, prenyl phenol is in a solid state, appearing as crystalline material.

Melting point (Celsius)
52.00
Melting point (Kelvin)
325.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
162.24g/mol
Molar mass
162.2360g/mol
Density
1.0133g/cm3
Appearence

Prenyl phenol appears as a white to light yellow crystalline solid. It has a distinct phenolic odor and may form crystalline needles when purified.

Comment on solubility

Solubility of 4-(3-methylbut-2-enyl)phenol

4-(3-methylbut-2-enyl)phenol, also known as a substituted phenolic compound, exhibits notable solubility properties that are essential to understand for its practical applications. Here are some key points regarding its solubility:

  • Polarity: The presence of both a hydrocarbon chain and a hydroxyl group indicates that 4-(3-methylbut-2-enyl)phenol has a distinctive balance between polar and non-polar characteristics. This affects its solubility in various solvents.
  • Solvent Compatibility:
    • Soluble in: Organic solvents like ethanol and acetone due to its hydrophobic hydrocarbon tail.
    • Insoluble in: Water, because of the significant hydrocarbon character which resists interaction with water molecules.
  • Concentration Effects: At higher concentrations, the solubility may be influenced by interactions of the molecules, leading to the potential for lower solubility due to aggregation or solute-solute interactions.

To emphasize, understanding the solubility of 4-(3-methylbut-2-enyl)phenol is crucial for its use in applications such as pharmaceuticals, where solubility in specific solvents can dictate the compound’s efficacy and formulation. Overall, the balance of hydrophobic and hydrophilic interactions plays a pivotal role in determining the solubility behavior of this compound.

Interesting facts

Interesting Facts About 4-(3-Methylbut-2-enyl)phenol

4-(3-Methylbut-2-enyl)phenol, also known as t-amylenol, is an intriguing compound within the realm of organic chemistry. This compound features a phenolic structure that offers unique properties and various applications.

Key Characteristics:

  • Natural Occurrence: This compound can be found in essential oils, particularly in plants like spearmint and peppermint. It contributes to the aromatic profile of these plants.
  • Flavor and Fragrance: Due to its pleasant scent, 4-(3-methylbut-2-enyl)phenol is often utilized in the food and cosmetic industries as a flavoring agent or fragrance component.
  • Antioxidant Properties: This compound has been studied for its potential antioxidant activities, which may help in reducing oxidative stress in biological systems.

Researchers are also exploring its role in various chemical reactions, particularly in the context of electrophilic substitution reactions. This property makes it a valuable building block in synthetic organic chemistry.

Application Potential:

  • Pharmaceuticals: The compound is being investigated for its potential therapeutic uses.
  • Chemical Synthesis: It may serve as a precursor in the synthesis of more complex organic molecules.

In summary, 4-(3-methylbut-2-enyl)phenol is not just a simple organic compound; its diverse applications and presence in nature make it a fascinating subject for further study in chemistry.

Synonyms
4-(3-methylbut-2-enyl)phenol
686-822-6
1200-09-5
PHENOL, p-(3-METHYL-2-BUTENYL)-
Phenol, 4-(3-methyl-2-butenyl)-
p-(3-Methyl-2-butenyl)phenol
4-(3-methylbut-2-en-1-yl)phenol
NSC 407855
BRN 1931271
p-prenylphenol
AI3-22827
4-(3-Methyl-2-butenyl)phenol
NSC407855
4-(3-Methylcrotyl)phenol
EC 686-822-6
WLN: QR D2UY1&1
4-(3,3-Dimethylallyl)phenol
SCHEMBL1153975
DTXSID60152650
4-(3-Methyl-2-butenyl)phenol #
4-(3-methyl-but-2-enyl)-phenol
AKOS024323127
NSC-407855
1-(4-Hydroxyphenyl)-3-methylbut-2-ene
NS00001877