Galloyl capsaicin
- 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
Identification
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:
- Development of new pharmaceuticals with enhanced efficacy.
- Exploration of natural product synthesis pathways.
- 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.