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Cinnamyl Cinnamate

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Identification
Molecular formula
C18H16O2
CAS number
122-69-0
IUPAC name
cinnamyl 3-phenylprop-2-enoate
State
State

Cinnamyl cinnamate is a solid at room temperature and can often exist in a crystalline form.

Melting point (Celsius)
62.00
Melting point (Kelvin)
335.15
Boiling point (Celsius)
375.00
Boiling point (Kelvin)
648.15
General information
Molecular weight
236.30g/mol
Molar mass
236.3030g/mol
Density
1.0863g/cm3
Appearence

Cinnamyl cinnamate is an off-white or pale yellow solid with a faint balsamic odor reminiscent of cinnamon. It is typically found in crystalline powder form.

Comment on solubility

Solubility of Cinnamyl 3-phenylprop-2-enoate

Cinnamyl 3-phenylprop-2-enoate, a delightful aromatic compound, often exhibits unique solubility characteristics due to its organic nature. Understanding its solubility is key to its application in various fields, such as in fragrances and food flavoring. Here are some insights into its solubility:

  • Solvent Compatibility: This compound is generally soluble in organic solvents like ethanol, methanol, and certain oils, owing to its hydrophobic properties.
  • Water Solubility: Cinnamyl 3-phenylprop-2-enoate is practically insoluble in water, which is a common trait for many large organic molecules, especially those with considerable hydrophobic regions.
  • Temperature Effects: The solubility may increase with temperature as it enhances the interaction between molecules, allowing for better dissolution in organic solvents.
  • pH Sensitivity: While cinnamyl 3-phenylprop-2-enoate does not show significant pH dependence, being neutral helps it maintain its solubility profile in various organic environments.

In summary, the solubility of cinnamyl 3-phenylprop-2-enoate is influenced by the choice of solvent, temperature, and its inherent chemical structure. This compound serves as a prime example of how solubility can affect the versatility of organic compounds in practical applications.

Interesting facts

Exploring Cinnamyl 3-phenylprop-2-enoate

Cinnamyl 3-phenylprop-2-enoate, a captivating compound in the realm of organic chemistry, is noteworthy for its applications and distinct structure. Here are some intriguing facts about this compound:

  • Cultural significance: This compound serves as a key component in the synthesis of various fragrances and flavoring agents. Its sweet, spicy aroma is reminiscent of cinnamon, making it valuable in the perfume and food industries.
  • Natural occurrences: Cinnamyl derivatives are often found in nature, particularly in essential oils derived from plants like cinnamon. Their natural origins add to their appeal in products aiming for a more holistic approach.
  • Reactivity: This compound showcases a unique reactivity profile, often engaging in chemical reactions such as polymerization. These reactions play a critical role in the development of new materials and polymers.
  • Research interest: Studies have indicated the potential of cinnamyl compounds in anti-inflammatory and antimicrobial research, paving the way for innovative medicines and health supplements.
  • Biotechnological applications: Due to its structure, cinnamyl 3-phenylprop-2-enoate can be modified enzymatically, making it an exciting candidate for biocatalysis in sustainable chemical processes.

As a compound that bridges the realms of chemistry, biology, and industry, cinnamyl 3-phenylprop-2-enoate exemplifies how organic compounds can not only provide benefits in their raw forms but can also lead to breakthroughs in various fields.

Synonyms
2-Propenoic acid, 3-phenyl-, 3-phenyl-2-propenyl ester
RefChem:482078
Cinnamic Acid Cinnamyl Ester
Cinnamyl cinnamate, mixture of isomers
3-phenylprop-2-en-1-yl 3-phenylprop-2-enoate
DTXSID7047647
cinnamyl 3-phenylprop-2-enoate
CBDivE_001756
SCHEMBL112366
orb1684698
CHEMBL3186867
2-Propenoic acid, 3-phenyl-, 3-phenyl-2-propenyl ester; Cinnamic acid, cinnamyl este
AKOS025244100
DB-041681
3-Phenylallyl cinnamate; 3-Phenyl-2-propen-1-yl 3-phenyl propenoate