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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
State
State

At room temperature, this compound is in a solid state. It is typically crystalline in nature and may exhibit a slight odor characteristic of phenolic compounds.

Melting point (Celsius)
67.00
Melting point (Kelvin)
340.00
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.00
General information
Molecular weight
308.14g/mol
Molar mass
308.1360g/mol
Density
1.1500g/cm3
Appearence

The compound generally appears as a yellow or orange solid at room temperature. It can have a slightly tacky texture depending on the specific conditions and purity of the sample. The color intensity may vary based on the source and any impurities that are present.

Comment on solubility

Solubility 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

The solubility of the compound represented by the formula C12H14O6 is an intriguing aspect that warrants attention. Understanding the solubility can provide insights into its behavior in various environments. Here are some key points regarding its solubility:

  • Polar vs. Nonpolar Characteristics: This compound contains multiple hydroxyl (-OH) functional groups and carbonyl (C=O) groups that often enhance solubility in polar solvents, such as water.
  • Hydrogen Bonding: The presence of hydroxyl groups suggests that the compound can participate in hydrogen bonding, which further facilitates solubility in polar media.
  • Hydrophobic Regions: The complex hydrocarbon structure indicates that there are segments of the molecule that may be hydrophobic (water-repelling), which can limit solubility in water but may promote solubility in organic solvents.
  • Temperature Dependence: Solubility may vary with temperature, generally increasing with higher temperatures for many organic compounds.
  • Practical Applications: Understanding its solubility can be crucial for its applications in fields such as pharmaceuticals, environmental science, and chemical manufacturing.

In summary, while this compound exhibits potential for solubility in polar solvents due to its functional groups, its complex structure may introduce challenges in certain environments, leading to variable solubility characteristics.

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.

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
CID 2432