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Cannabidiol B (CBD)

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Identification
Molecular formula
C21H30O3
CAS number
13956-29-1
IUPAC name
5,6,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-3-vinyl-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-1-one
State
State
Cannabidiol B (CBD) is typically in a solid state at room temperature when pure. However, it is often encountered in oil form, resulting in a liquid state for practical uses and applications.
Melting point (Celsius)
66.00
Melting point (Kelvin)
339.15
Boiling point (Celsius)
187.00
Boiling point (Kelvin)
460.15
General information
Molecular weight
314.46g/mol
Molar mass
314.4640g/mol
Density
0.9350g/cm3
Appearence

Cannabidiol typically appears as a colorless crystalline solid in pure form. However, it is commonly available as an oil-based solution, which can range from light to dark amber in color, depending on the purity and the specific formulation. The oil may also be cloudy if not fully refined or if other natural constituents are present.

Comment on solubility

Solubility of 5,6,10b-Trihydroxy-3,4a,7,7,10a-pentamethyl-3-vinyl-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-1-one (C21H30O3)

The solubility of the compound 5,6,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-3-vinyl-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-1-one can be characterized by several key points:

  • Polarity: The presence of multiple hydroxyl (-OH) groups suggests that this compound may exhibit a degree of polarity, which can enhance its solubility in polar solvents such as water.
  • Non-polar characteristics: However, the high degree of methyl substitution and the hydrophobic portions of the molecule may limit solubility in more polar media.
  • Solvent compatibility: This compound might be more soluble in organic solvents such as ethanol, acetone, or dichloromethane due to its hydrophobic characteristics.
  • Temperature effects: Like many organic compounds, the solubility can also increase with temperature, allowing for better dissolution at elevated temperatures.

In conclusion, the solubility of C21H30O3 is likely influenced by a balance between its polar and non-polar characteristics, making it a compound that can be soluble in selected solvents based on both chemical structure and environmental conditions. To truly assess its solubility, experimental data would be vital.

Interesting facts

Exploring 5,6,10b-Trihydroxy-3,4a,7,7,10a-Pentamethyl-3-vinyl-5,6,6a,8,9,10-Hexahydro-2H-Benzo[f]chromen-1-one

This fascinating compound, known for its complex structure, belongs to a class of chemicals that exhibit interesting biological activities. Here are some intriguing facts that highlight its significance:

  • Structural Complexity: The intricate arrangement of substituents on the benzochromene core contributes to its unique chemical reactivity and biological properties.
  • Natural Origins: Compounds similar to this one are often derived from natural sources, including plants, where they may play roles in ecological interactions or defense mechanisms.
  • Potential Applications: Research has indicated that this compound could have applications in various fields, including medicine and materials science. Its derivatives may possess antioxidant, anti-inflammatory, or anticancer properties, making it a subject of interest for drug development.
  • Vinyl Group Significance: The presence of a vinyl group in its structure allows for potential polymerization, opening avenues for creating new materials with desirable properties.
  • Synthesis Challenges: The multi-step synthesis of this compound showcases the challenges chemists face when navigating complex organic molecules, requiring advanced techniques in organic synthesis.

As science continues to evolve, the study of compounds like 5,6,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-3-vinyl-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-1-one remains pivotal for unlocking new possibilities in chemistry. In the words of famous chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This compound certainly exemplifies this philosophy, inspiring ongoing research and exploration.