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Cinnamylvanillin

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Identification
Molecular formula
C18H18O4
CAS number
6539-73-3
IUPAC name
2-phenylethyl 3-(3,4-dimethoxyphenyl)prop-2-enoate
State
State

At room temperature, this compound is typically in a solid state due to its crystalline structure.

Melting point (Celsius)
70.00
Melting point (Kelvin)
343.15
Boiling point (Celsius)
200.00
Boiling point (Kelvin)
473.15
General information
Molecular weight
314.35g/mol
Molar mass
314.3630g/mol
Density
1.1118g/cm3
Appearence

Cinnamylvanillin is typically a yellowish crystalline solid that is slightly soluble in water. It can have a characteristic aromatic odor reminiscent of vanilla and cinnamaldehyde.

Comment on solubility

Solubility of 2-phenylethyl 3-(3,4-dimethoxyphenyl)prop-2-enoate (C18H18O4)

The solubility of 2-phenylethyl 3-(3,4-dimethoxyphenyl)prop-2-enoate can be described as follows:

  • General Solubility: This compound is generally considered to be poorly soluble in water due to its extensive aromatic structure, which tends to be hydrophobic.
  • Polar Solvents: It may demonstrate moderate solubility in polar organic solvents such as ethanol and methanol, primarily due to the presence of the ester functional group which can interact favorably with polar solvents.
  • Non-Polar Solvents: In non-polar solvents, its solubility is likely to be higher, as the non-polar components of the molecule can effectively participate in van der Waals interactions.

When considering the solubility:

  • In polar environments, hydrophobic interactions dominate, leading to decreased solubility.
  • In non-polar environments, dispersion forces allow for enhanced solute-solvent interactions.

In summary, the solubility behavior of this compound is influenced significantly by the balance between its large aromatic framework and its ester moiety, making it more suited for organic solvents than for aqueous solutions.

Interesting facts

Interesting Facts about 2-Phenylethyl 3-(3,4-Dimethoxyphenyl)prop-2-enoate

2-Phenylethyl 3-(3,4-dimethoxyphenyl)prop-2-enoate is a fascinating compound that showcases the intricate world of organic chemistry. This ester is derived from two aromatic rings, giving it unique structural and chemical properties. Here are some intriguing aspects of this compound:

  • Versatile Applications: This compound is primarily studied for its potential applications in pharmaceuticals, particularly as a precursor in the synthesis of biologically active molecules.
  • Flavor and Fragrance: The phenolic structure suggests that it may exhibit pleasant aromatic properties, which can be valuable for use in the flavor and fragrance industry.
  • Potential Biological Activity: Compounds featuring methoxy groups have been noted for their various biological activities, including antioxidant and anti-inflammatory effects. This leads to ongoing research into the medicinal properties of 2-phenylethyl 3-(3,4-dimethoxyphenyl)prop-2-enoate.
  • Resonance Stabilization: The presence of the methoxy groups impacts the electron distribution within the aromatic rings, enhancing the compound's stability and chemical reactivity through resonance effects.

In the words of renowned chemist Linus Pauling, “The best way to have a good idea is to have a lot of ideas.” The study of compounds like 2-phenylethyl 3-(3,4-dimethoxyphenyl)prop-2-enoate exemplifies this philosophy, as each investigation opens doors to new possibilities and applications in chemistry.

As the field of organic chemistry continues to evolve, the exploration of candidates such as this compound contributes to an ever-growing understanding of how we can manipulate chemical structures for innovative uses.

Synonyms
Caffeic Acid Dimethyl Ether Phenethyl Ester
145551-14-0
2-phenylethyl 3-(3,4-dimethoxyphenyl)prop-2-enoate
AKOS030239800
H27784