Skip to main content

4-Phenyl-3-buten-2-ol

ADVERTISEMENT
Identification
Molecular formula
C10H12O
CAS number
122-97-4
IUPAC name
4-phenylbut-3-en-2-ol
State
State

At room temperature, 4-Phenyl-3-buten-2-ol is in a liquid state. Its relatively low melting point contributes to it remaining a liquid under standard conditions.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
148.20g/mol
Molar mass
148.2020g/mol
Density
0.9787g/cm3
Appearence

4-Phenyl-3-buten-2-ol is typically a clear to pale yellow liquid. It may have a slightly oily appearance and a mild fragrance due to its functional groups and aromatic ring.

Comment on solubility

Solubility of 4-phenylbut-3-en-2-ol

4-phenylbut-3-en-2-ol, a compound known for its unique structural formula, exhibits particular solubility characteristics that are worth noting. In organic solvents, this compound tends to show a notable solubility due to its structural composition.

Key Points on Solubility:

  • Solvent Influence: 4-phenylbut-3-en-2-ol is more soluble in polar organic solvents like ethanol, methanol, and acetone.
  • Non-Polar Solvents: Its solubility decreases in non-polar solvents, suggesting it prefers environments where hydrogen bonding can occur.
  • Temperature Effects: Increasing temperature can enhance solubility in many solvents, leading to improved compatibility for various applications.

As a result, understanding the solubility profile of 4-phenylbut-3-en-2-ol is essential for its use in chemical reactions and applications. Emphasizing the solvent choice can significantly impact the efficiency of processes involving this compound. As always, it is vital to consider how the molecular structure influences solubility, echoing the fundamental principle in chemistry: "Like dissolves like."

Interesting facts

Exploring 4-phenylbut-3-en-2-ol

The compound 4-phenylbut-3-en-2-ol is a fascinating molecule that displays unique characteristics due to its structural features. This compound is classified as an allylic alcohol, which means it contains both a double bond and an alcohol functional group in its structure. Here are some interesting facts about this compound:

  • Versatile Synthetic Pathways: 4-phenylbut-3-en-2-ol can be synthesized through various methods, including the reaction of phenylacetic acid derivatives with suitable reagents. This versatility allows chemists to tailor its synthesis based on available starting materials.
  • Potential in Organic Synthesis: The compounds that share a similar structural backbone to 4-phenylbut-3-en-2-ol are often used in organic synthesis as intermediates or building blocks for more complex pharmaceuticals and agrochemicals.
  • Biological Activity: Some derivatives of allylic alcohols have shown biological activity, including antimicrobial and antifungal properties, making 4-phenylbut-3-en-2-ol an interesting candidate for further investigation in medicinal chemistry.
  • Importance in Material Science: Researchers are exploring the potential applications of such compounds in material science, particularly in the development of polymers and other advanced materials. 4-phenylbut-3-en-2-ol could play a role in enhancing material properties.

As a member of the allylic alcohol family, 4-phenylbut-3-en-2-ol sits at the intersection of fascinating chemistry and practical applications. Its study not only enriches our understanding of alcohols and their reactivity but also opens avenues for new discoveries in various fields. As chemists often quote, “The beauty of chemistry lies in its intricacies.”

Synonyms
4-phenylbut-3-en-2-ol
17488-65-2
3-Buten-2-ol, 4-phenyl-
4-Phenyl-3-buten-2-ol
Methylstyrylcarbinol
4-phenyl-3-buten-2ol
4-phenyl-but-3-ene-2-ol
DTXSID90864779
WLZ3162
DB-367944
NS00084969