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trans-Cinnamic acid

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Identification
Molecular formula
C9H8O2
CAS number
140-10-3
IUPAC name
3-(4-phenylphenyl)prop-2-enoic acid
State
State

At room temperature, trans-Cinnamic acid is in a solid state.

Melting point (Celsius)
133.00
Melting point (Kelvin)
406.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
148.16g/mol
Molar mass
148.1640g/mol
Density
1.2470g/cm3
Appearence

trans-Cinnamic acid appears as a white crystalline solid. It often forms needle-shaped crystals that are colorless or white.

Comment on solubility

Solubility of 3-(4-phenylphenyl)prop-2-enoic acid (C9H8O2)

3-(4-phenylphenyl)prop-2-enoic acid, also known as a type of styrene derivative, exhibits unique solubility characteristics that are significant for its applications. The solubility of this compound can be influenced by several factors:

  • Polarity: Being an aromatic compound with a carboxylic acid functional group, it demonstrates moderate polarity. This affects its solubility in various solvents.
  • Solvent Type: Generally, 3-(4-phenylphenyl)prop-2-enoic acid is soluble in organic solvents such as ethanol and acetone, while its solubility in water is limited due to the hydrophobic nature of the phenyl groups.
  • Temperature: Like many organic compounds, increasing temperature can enhance solubility, allowing for better interaction with solvents.

In practical terms, this compound may be described as:

  • Partially soluble in water, making it less suitable for aqueous applications.
  • Soluble in most organic solvents, which is advantageous for synthesis and processing.

Understanding its solubility profile is crucial for anyone looking to employ 3-(4-phenylphenyl)prop-2-enoic acid in research or industrial settings, as it directly influences the compound's behavior in various chemical reactions.

Interesting facts

Interesting Facts about 3-(4-phenylphenyl)prop-2-enoic acid

3-(4-phenylphenyl)prop-2-enoic acid, commonly known as a derivative of cinnamic acid, showcases a fascinating structure that combines aromatic rings with a prop-2-enoic acid functional group. Here are some intriguing aspects of this compound:

  • Structural Intricacy: The presence of two phenyl groups in its structure gives this compound unique geometrical characteristics, potentially affecting its reactivity and interactions with other molecules.
  • Biological Significance: Compounds like this one are often studied for their biological activities. Notably, some derivatives of cinnamic acid exhibit anti-inflammatory and antioxidant properties.
  • Applications in Material Science: The property of this acid derivative makes it an interesting candidate for applications in the development of organic materials, such as polymers and dyes.
  • Research Potential: Ongoing research into compounds similar to 3-(4-phenylphenyl)prop-2-enoic acid suggests their role in drug design and synthesis due to their complex structure.

In summary, 3-(4-phenylphenyl)prop-2-enoic acid is not only remarkable for its chemical structure but also for the various applications and biological activities it may possess. As quotes from chemists often say, "The beauty of chemistry lies in discovering the potential of complex molecular structures." Exploring such compounds can unlock new paths in both medicinal and industrial chemistry.

Synonyms
3-(4-phenylphenyl)prop-2-enoic acid
(2E)-3-biphenyl-4-ylacrylic acid
SCHEMBL165795
3-biphenyl-4-yl-acrylic acid
SCHEMBL1510082
SCHEMBL1510673
SCHEMBL27961597
DMJDEZUEYXVYNO-UHFFFAOYSA-N
DTXSID901278241
AKOS030239784
(Z)-3-(4-phenylphenyl)prop-2-enoic acid
DB-041955
D78177
3-[1,1a(2)-Biphenyl]-4-yl-2-propenoic acid