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Quassin

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Identification
Molecular formula
C22H28O6
CAS number
76-78-8
IUPAC name
(1S,5aR)-1-hydroxy-1,9a,11a-trimethyl-2,3,3a,3b,4,5,5a,8,9,9b,10,11-dodecahydroindeno[5,4-f]chromen-7-one
State
State

At room temperature, quassin exists as a solid.

Melting point (Celsius)
205.00
Melting point (Kelvin)
478.15
Boiling point (Celsius)
176.00
Boiling point (Kelvin)
449.15
General information
Molecular weight
504.52g/mol
Molar mass
504.5190g/mol
Density
1.3403g/cm3
Appearence

Quassin appears as a white crystalline substance. It is often found in the bark of certain tropical trees and is known for its intensely bitter taste.

Comment on solubility

Solubility Characteristics of (1S,5aR)-1-hydroxy-1,9a,11a-trimethyl-2,3,3a,3b,4,5,5a,8,9,9b,10,11-dodecahydroindeno[5,4-f]chromen-7-one

The solubility of (1S,5aR)-1-hydroxy-1,9a,11a-trimethyl-2,3,3a,3b,4,5,5a,8,9,9b,10,11-dodecahydroindeno[5,4-f]chromen-7-one is an intriguing aspect of this compound. Its solubility can be influenced by a variety of factors:

  • Polarity: The presence of hydroxyl (-OH) functional groups may enhance solubility in polar solvents such as water.
  • Hydrophobic nature: The overall structure, with multiple methyl groups and the dodecahydroindeno framework, suggests a tendency towards hydrophobic behavior, potentially limiting solubility in aqueous environments.
  • Temperature: Increased temperatures might enhance solubility, as is common with many organic compounds.
  • pH Levels: The ionization of the hydroxyl group at varying pH levels can significantly affect solubility.

In practical applications, the solubility of compounds like this one can be critical. Depending on its solubility profile:

  • It may find use in pharmaceuticals, where solubility affects bioavailability.
  • Its solubility can determine its behavior in biological systems, impacting absorption and distribution.

In conclusion, while certain aspects suggest enhanced solubility due to polar groups, the large hydrophobic components of the compound could lead to limited solubility in polar solvents. This duality makes (1S,5aR)-1-hydroxy-1,9a,11a-trimethyl-2,3,3a,3b,4,5,5a,8,9,9b,10,11-dodecahydroindeno[5,4-f]chromen-7-one a compound worth investigating further in terms of solubility dynamics.

Interesting facts

Interesting Facts about (1S,5aR)-1-hydroxy-1,9a,11a-trimethyl-2,3,3a,3b,4,5,5a,8,9,9b,10,11-dodecahydroindeno[5,4-f]chromen-7-one

(1S,5aR)-1-hydroxy-1,9a,11a-trimethyl-2,3,3a,3b,4,5,5a,8,9,9b,10,11-dodecahydroindeno[5,4-f]chromen-7-one is a fascinating compound with a unique structure and intriguing properties. Here are some noteworthy points about this compound:

  • Synthetic Versatility: The complex structure of this compound allows for various synthetic routes, making it a crucial building block in organic chemistry.
  • Biological Activity: Research indicates that compounds like this one may exhibit significant biological activities, potentially acting as antioxidants or anti-inflammatory agents.
  • Natural Occurrence: Similar structures can be found in several natural products, highlighting this compound's potential importance in the realm of natural chemistry.
  • Chirality: With specific stereochemical descriptions, chirality plays a significant role in the behavior of this compound, influencing its interactions in biological systems.

In research and applications, the intricate structure of this compound presents opportunities for novel derivative synthesis, enhancing our understanding of similar organic compounds in therapeutic contexts. Overall, the study of (1S,5aR)-1-hydroxy-1,9a,11a-trimethyl-2,3,3a,3b,4,5,5a,8,9,9b,10,11-dodecahydroindeno[5,4-f]chromen-7-one not only enriches our knowledge of its unique properties but also emphasizes the broader significance of similar molecular frameworks in advancing scientific discovery.