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3-(4-tert-butylphenyl)butanal

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Identification
Molecular formula
C14H20O
CAS number
80841-78-7
IUPAC name
3-(4-tert-butylphenyl)butanal
State
State
At room temperature, 3-(4-tert-butylphenyl)butanal is typically found in a liquid state.
Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
269.10
Boiling point (Kelvin)
542.25
General information
Molecular weight
188.32g/mol
Molar mass
188.2800g/mol
Density
0.9056g/cm3
Appearence

This compound is generally observed as a colorless to pale yellow liquid. It has a characteristic odor, often used in fragrance formulations due to its aromatic properties.

Comment on solubility

Solubility of 3-(4-tert-butylphenyl)butanal

The solubility of 3-(4-tert-butylphenyl)butanal, a compound with an interesting structure, can be influenced by several factors including its molecular weight, polarizability, and intermolecular interactions.

Key points regarding its solubility:

  • Polar and Nonpolar Characteristics: This compound features a bulky tert-butyl group which is largely hydrophobic, promoting solubility in nonpolar solvents.
  • Solvents: It is likely to dissolve well in organic solvents such as:
    • Hexane
    • Toluene
    • Chloroform
  • Water Solubility: However, due to its nonpolar characteristics, it has poor solubility in water, making it less favorable for aqueous reactions.

In conclusion, while 3-(4-tert-butylphenyl)butanal exhibits favorable solubility in nonpolar solvents, its interaction with polar solvents like water is significantly reduced due to the presence of the bulky hydrophobic group. This underlines the importance of understanding a compound's structure when predicting its solubility behavior in various media.

Interesting facts

Interesting Facts about 3-(4-tert-butylphenyl)butanal

3-(4-tert-butylphenyl)butanal, often known for its intriguing structure, is a compound that captures the attention of chemists and students alike. Here are some fascinating aspects about this organic molecule:

  • Structural Composition: This compound features a distinctive butanal group, characterized by an aldehyde functional group connected to a four-carbon chain. The addition of a 4-tert-butylphenyl substituent enhances its structural complexity and steric hindrance, making it a subject of study in diverse chemical reactions.
  • Applications in Synthesis: 3-(4-tert-butylphenyl)butanal serves as an important building block in organic synthesis. Its unique properties allow it to participate in various chemical reactions, including aldol condensations and other coupling reactions, thus paving the way for the creation of more complex molecules.
  • Importance in Material Science: The compound is particularly relevant in the field of materials science, where it may be utilized in the formulation of polymers and resins that possess improved thermal stability and mechanical properties.
  • Biological Significance: Research into this compound has suggested potential biological activities. As scientists explore its derivatives, there may be promising implications in the development of pharmaceutical agents or agrochemicals.

As chemists continue to investigate the properties and potential uses of 3-(4-tert-butylphenyl)butanal, its significance in both synthetic and applied chemistry cannot be overlooked. The implications of this compound extend beyond the laboratory, inviting innovation and discovery within various scientific disciplines.

Synonyms
SCHEMBL166235
3-(4-tert.-Butylphenyl)butanal