Skip to main content

Cinnamyl acrylate

ADVERTISEMENT
Identification
Molecular formula
C12H12O2
CAS number
103-26-4
IUPAC name
allyl 3-phenylprop-2-enoate
State
State

At room temperature, cinnamyl acrylate is typically in a liquid state.

Melting point (Celsius)
-11.00
Melting point (Kelvin)
262.15
Boiling point (Celsius)
271.00
Boiling point (Kelvin)
544.15
General information
Molecular weight
188.22g/mol
Molar mass
188.2210g/mol
Density
1.0370g/cm3
Appearence

Cinnamyl acrylate appears as a colorless to pale yellow liquid. It is known for its pleasant floral odor, which makes it useful in perfumery and fragrances.

Comment on solubility

Solubility of Allyl 3-Phenylprop-2-enoate

Allyl 3-phenylprop-2-enoate, a compound known for its distinctive structure, presents interesting solubility characteristics that can be understood through a few key points:

  • Polar vs. Nonpolar Solubility: As an organic ester, allyl 3-phenylprop-2-enoate exhibits a tendency to dissolve in nonpolar solvents. This solubility can be attributed to the nonpolar hydrocarbon chains present in its structure.
  • Sensitivity to Temperature: The solubility of this compound may increase with rising temperatures, making it more soluble in nonpolar organic solvents as the solution's kinetic energy increases.
  • Common Solvents: It is typically soluble in solvents such as hexane, toluene, and chloroform. This behavior is consistent with many similar organic compounds that favor nonpolar environments.

However, friendliness with water is limited: allyl 3-phenylprop-2-enoate is considered to be practically insoluble in water due to the strong hydrogen bonding nature of water molecules, which cannot effectively interact with the nonpolar regions of the compound.

In summary, the solubility of allyl 3-phenylprop-2-enoate can be convincingly described as:

  1. Well soluble in nonpolar organic solvents.
  2. Insoluble or nearly insoluble in water.
  3. Temperature-dependent solubility, favoring higher temperatures for better dissolution in nonpolar solvents.

The intricate balance of polar and nonpolar interactions plays a crucial role in understanding how allyl 3-phenylprop-2-enoate behaves in various environments.

Interesting facts

Interesting Facts About Allyl 3-phenylprop-2-enoate

Allyl 3-phenylprop-2-enoate is an intriguing organic compound known for its unique structure and versatile applications in chemistry. Here are some interesting insights about this compound:

  • Structure and Functional Groups: The compound features a distinct allyl group that contributes to its reactivity. This combination with a phenyl group and an enoate functional group makes it a subject of study for organic chemists interested in substitution reactions.
  • Culinary and Fragrance Uses: Thanks to its aromatic properties, allyl 3-phenylprop-2-enoate is sometimes employed in the formulation of flavors and fragrances. Its pleasing scent profile makes it a candidate for potential use in perfumes and food additives.
  • Polymerization Potential: This compound can serve as a monomer in various polymerization processes. Polymers derived from allyl 3-phenylprop-2-enoate may possess desirable qualities such as flexibility and durability, which can be useful in materials science.
  • Biological Activities: Research indicates that compounds similar to allyl 3-phenylprop-2-enoate exhibit various biological activities. Studies are ongoing into its potential applications in medicinal chemistry and as a scaffold for new pharmaceuticals.
  • Visual Aesthetics in Laboratory: Working with allyl 3-phenylprop-2-enoate can be a visual treat in the laboratory. Chemists often find the process of synthesizing and purifying such vibrant compounds both rewarding and educational.

In conclusion, allyl 3-phenylprop-2-enoate illustrates the fascinating interplay between structure, reactivity, and application in the chemical sciences. Its role in flavoring, fragrance, and potential for further research exemplifies how organic compounds can transcend simple chemical composition to become vital parts of both industry and research.

Synonyms
prop-2-enyl 3-phenylprop-2-enoate
ALLYLCINNAMATE
AKOS028110007
DB-003582