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Isobutyl cinnamate

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Identification
Molecular formula
C13H16O2
CAS number
122-67-8
IUPAC name
isobutyl 3-phenylprop-2-enoate
State
State

At room temperature, isobutyl cinnamate is typically in a liquid state.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
266.50
Boiling point (Kelvin)
539.70
General information
Molecular weight
206.27g/mol
Molar mass
206.2690g/mol
Density
0.9837g/cm3
Appearence

Isobutyl cinnamate is a colorless to pale yellow liquid. It possesses a characteristic floral and balsamic aroma.

Comment on solubility

Solubility of Isobutyl 3-phenylprop-2-enoate

Isobutyl 3-phenylprop-2-enoate, a compound with the formula C13H16O2, exhibits unique solubility characteristics that merit attention. Understanding the solubility profile of this compound is essential for various industrial and chemical applications. Here are some key points:

  • Solvent Compatibility: Isobutyl 3-phenylprop-2-enoate tends to exhibit greater solubility in organic solvents such as ethanol, ether, and acetone, while being less soluble in water.
  • Polarity Factors: The presence of the phenyl group and the ester functionality influences its polarity, leading to enhanced solubility in non-polar to slightly polar solvents.
  • Temperature Effects: Solubility generally increases with temperature, which could significantly affect its behavior during chemical reactions or extractions.
  • Kinetic Considerations: The rate of dissolution can vary based on factors such as agitation, concentration of solution, and surface area of the compound.

In summary, the solubility of isobutyl 3-phenylprop-2-enoate is influenced by both its molecular structure and the medium in which it is dissolved. The compound's preference for organic solvents makes it a versatile agent in various chemical processes.

Interesting facts

Interesting Facts About Isobutyl 3-phenylprop-2-enoate

Isobutyl 3-phenylprop-2-enoate, an intriguing compound in organic chemistry, falls under the category of unsaturated esters. This compound is known for its unique structure and versatility in various applications. Here are some captivating aspects of this chemical:

  • Structural Complexity: The molecule exhibits a mixture of straight-chain and aromatic components, giving it interesting chemical properties that allow it to engage in multiple reactions.
  • Uses in Synthesis: Often utilized in organic synthesis, this compound acts as a valuable intermediate. It can be transformed into various derivatives, broadening its utility in the field of chemical manufacturing.
  • Perfume Industry: Its aromatic characteristics make isobutyl 3-phenylprop-2-enoate a candidate for use in fragrance formulations. The pleasant scent can be attributed to its phenyl group, which contributes to floral and fruity notes.
  • Polymer Chemistry: This compound may serve as a monomer for polymeric materials, which could possess unique properties like improved flexibility and durability, making them useful in developing various products.
  • Environmental Considerations: Like many esters, its behavior in the environment can be of interest to chemists focusing on biodegradability and ecological impact, including its potential pathways for degradation.

As a student or researcher in chemistry, exploring the diverse roles of compounds like isobutyl 3-phenylprop-2-enoate offers a fascinating glimpse into the interplay of structure and function in the world of chemistry.

Synonyms
DTXSID2047646
isobutyl 3-phenylprop-2-enoate
CBDivE_001758
SCHEMBL868715
orb2893591
CHEMBL3188070
IQZUZPKOFSOVET-UHFFFAOYSA-N
DB-041679