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methyl caffeate

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Identification
Molecular formula
C10H10O4
CAS number
3870-67-5
IUPAC name
methyl 3-(2,5-dihydroxyphenyl)prop-2-enoate
State
State

At room temperature, methyl caffeate is typically found in a solid state. It is often stored at room temperature, away from moisture and sunlight to maintain its stability and prevent degradation.

Melting point (Celsius)
174.00
Melting point (Kelvin)
447.20
Boiling point (Celsius)
411.40
Boiling point (Kelvin)
684.60
General information
Molecular weight
194.18g/mol
Molar mass
194.1840g/mol
Density
1.3216g/cm3
Appearence

Methyl caffeate is typically presented as a crystalline powder which is light yellow in color. It is often used as an intermediate in organic synthesis and has a precise crystalline structure that is visually discernible under magnification.

Comment on solubility

Solubility of Methyl 3-(2,5-dihydroxyphenyl)prop-2-enoate (C10H10O4)

Methyl 3-(2,5-dihydroxyphenyl)prop-2-enoate is a compound that exhibits a unique solubility behavior influenced by its functional groups. Understanding its solubility is key to determining its potential applications. Here are some insights:

  • Polar vs. Non-Polar Solvents: This compound is expected to show reasonable solubility in polar solvents like methanol and ethanol due to the presence of hydroxyl (–OH) groups that can form hydrogen bonds.
  • Hydrophobic Interactions: The hydrophobic phenyl ring may limit its solubility in purely non-polar solvents, indicating that “like dissolves like.”
  • Concentration Effects: At higher concentrations, the solubility may decrease due to potential aggregation of the molecules, which can lead to precipitation.

To summarize, methyl 3-(2,5-dihydroxyphenyl)prop-2-enoate shows variable solubility depending on the solvent used, highlighting its **dual nature** as both hydrophilic and hydrophobic. Further studies into its solubility characteristics could reveal more about its behavior in different environments.

Interesting facts

Interesting Facts About Methyl 3-(2,5-Dihydroxyphenyl)prop-2-enoate

Methyl 3-(2,5-dihydroxyphenyl)prop-2-enoate, commonly referred to in scientific literature, is a fascinating compound belonging to the class of esters. This compound exhibits unique characteristics and potential applications that make it an interesting subject of study in the field of chemistry.

Key Highlights

  • Structure and Functional Groups: The compound features a central prop-2-enoate structure, which includes an ester functional group. Additionally, the presence of two hydroxyl groups in the phenyl ring contributes to its reactivity and interaction with biological systems.
  • Biological Significance: The hydroxyl groups make this compound a candidate for various biological activities. Compounds with hydroxyl substituents are known to engage in hydrogen bonding, potentially enhancing their medicinal properties.
  • Research Applications: Methyl 3-(2,5-dihydroxyphenyl)prop-2-enoate may serve as a precursor for synthesizing more complex molecules in organic chemistry, highlighting its utility in chemical synthesis and material science.
  • Potential Uses: This compound could find applications in cosmetics, pharmaceuticals, and agrochemicals due to its unique structure and functional properties, warranting further exploration in these industries.

As students and researchers delve into the study of methyl 3-(2,5-dihydroxyphenyl)prop-2-enoate, they may uncover exciting insights about its reactivity, synthesis pathways, and potential therapeutic applications. In the words of a noted chemist, "Each compound tells a story of its formation and potential." This sentiment rings particularly true for such a multifaceted compound.

Synonyms
methyl (E)-3-(2,5-dihydroxyphenyl)acrylate
3-(2,5-dihydroxyphenyl)-2-propenoic acid methyl ester
HMS3266M18
AKOS025243609
DB-054420
M2520
Q27165237