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
Molecular Weight
194.18g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3216g/cm3
Synonyms
methyl (E)-3-(2, 5-dihydroxyphenyl)acrylate
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.

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