Galloyl capsaicin

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Identification

Molecular formula
C12H14O6
CAS Number
.104408-27-1
IUPAC Name
2-[(12-hydroxy-1,3,11,24,31,41,44-heptamethyl-39-oxo-2,6,10,15,19,25,29,34,38,43,47-undecaoxaundecacyclo[26.22.0.03,26.05,24.07,20.09,18.011,16.030,48.033,46.035,44.037,42]pentaconta-21,40-dien-14-yl)methyl]prop-2-enal
Molecular Weight
308.14g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1500g/cm3
Synonyms
2-[(12-Hydroxy-1, 3, 11, 24, 31, 41, 44-heptamethyl-39-oxo-2, 6, 10, 15, 19, 25, 29, 34, 38, 43, 47-undecaoxaundecacyclo[26.22.0.03, 26.05, 24.07, 20.09, 18.011, 16.030, 48.033, 46.035, 44.037, 42]pentaconta-21, 40-dien-14-yl)methyl]prop-2-enal
Interesting facts

Interesting Facts about 2-[(12-hydroxy-1,3,11,24,31,41,44-heptamethyl-39-oxo-2,6,10,15,19,25,29,34,38,43,47-undecaoxaundecacyclo[26.22.0.03,26.05,24.07,20.09,18.011,16.030,48.033,46.035,44.037,42]pentaconta-21,40-dien-14-yl)methyl]prop-2-enal

This compound is a fascinating example of complex organic chemistry, showcasing the diversity and intricacy of molecular structures. Known for its unique structure and numerous functional groups, it offers a myriad of potential applications and insights into chemical behavior.

Key Attributes:

  • Hydroxyl Group: The presence of the hydroxyl (-OH) group implicates the compound in various chemical reactions, often enhancing its reactivity and solubility in biological systems.
  • Oxoketene Structure: Its incorporation of an oxo group suggests that it could engage in both nucleophilic and electrophilic reactions, which are crucial in organic synthesis.
  • Complexity: This compound features a *polycyclic framework*, contributing to its interesting stereochemical properties that can influence interaction with biological molecules.

Moreover, the molecular name reveals a chain of intriguing functionalities and intricate bonding patterns, suggesting that research into such compounds may lead to valuable applications in medicinal chemistry, such as:

  1. Development of new pharmaceuticals with enhanced efficacy.
  2. Exploration of natural product synthesis pathways.
  3. Behavioral studies in catalysis utilizing the compound's reactive centers.

As with other complex organic compounds, studying the synthesis and reactivity of 2-[(12-hydroxy-1,3,11,24,31,41,44-heptamethyl-39-oxo-2,6,10,15,19,25,29,34,38,43,47-undecaoxaundecacyclo[26.22.0.03,26.05,24.07,20.09,18.011,16.030,48.033,46.035,44.037,42]pentaconta-21,40-dien-14-yl)methyl]prop-2-enal not only challenges our understanding of chemical bonding but also highlights the boundless opportunities that lie within organic synthesis.

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