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Tetrahydrocannabinol acetate

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Identification
Molecular formula
C23H34O5
CAS number
23132-17-4
IUPAC name
(6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-3-vinyl-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-5-yl) acetate
State
State

At room temperature, tetrahydrocannabinol acetate is typically an oily liquid. Due to its viscous nature, it might sometimes appear as a sticky, resinous substance.

Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
157.00
Boiling point (Kelvin)
430.15
General information
Molecular weight
384.54g/mol
Molar mass
384.5390g/mol
Density
1.0000g/cm3
Appearence

Tetrahydrocannabinol acetate usually appears as a viscous oil. It can also be found in a resinous form depending on its extraction and preparation. The color can vary from clear to amber-like but usually is a light yellow or pale shade.

Comment on solubility

Solubility of (6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-3-vinyl-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-5-yl) acetate

The solubility of this complex organic compound, C23H34O5, can be influenced by several factors owing to its unique structure. Here are some pertinent details regarding its solubility characteristics:

  • Polar vs. Non-Polar Solvents: Due to the presence of multiple hydroxy groups, one might expect a higher solubility in polar solvents such as water or alcohols. However, the overall non-polar hydrocarbon framework can also decrease solubility in highly polar environments.
  • Concentration Effects: As with many organic compounds, increasing the temperature can often enhance solubility, particularly in organic solvents.
  • pH Sensitivity: The solubility of hydroxy compounds can be affected by the pH of the solution. In a lower pH (acidic) environment, the compound’s functional groups may protonate, potentially leading to altered solubility behavior.
  • Crystalline Structure: If the compound forms a stable crystalline structure, its solubility may be significantly lower in comparison to an amorphous form. This factor could play an essential role in how well it dissolves in various solvents.

In conclusion, while the unique structure suggests potential for solubility in certain solvents, predicting the exact solubility behavior of (6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-3-vinyl-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-5-yl) acetate requires careful examination of these influencing factors. As emphasized by scholars, "the specific conditions of solvation play a crucial role in understanding solubility profiles." Thus, experimental data will be vital for accurate solubility determination.

Interesting facts

Interesting Facts About (6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-3-vinyl-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-5-yl) Acetate

Commonly known for its complex structure, the compound (6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-3-vinyl-5,6,6a,8,9,10-hexahydro-2H-benzo[f]chromen-5-yl) acetate exhibits intriguing characteristics that warrant a closer look. Here are some key insights:

  • Natural Origins: This compound is often derived from naturally occurring products, particularly those associated with plant sources, which contributes to its ecological significance.
  • Structural Complexity: The structure of this compound contains multiple hydroxy groups, contributing to its potential reactivity and interaction with various biological systems.
  • Potential Applications: Research is ongoing into its use in pharmaceuticals due to its possible bioactive properties, including anti-inflammatory and antioxidant activities.
  • Chemical Behavior: With its notable vinyl and acetate functional groups, the compound demonstrates interesting chemical behavior that can be valuable in synthetic applications.
  • Heterocyclic Nature: The benzochromene framework presents opportunities for exploring new reactions unique to heterocyclic compounds.

As highlighted by one prominent chemical researcher, “Compounds like these hold the keys to unlocking advanced therapeutic strategies and materials science.” Thus, the ongoing study of this compound not only enhances our understanding of complex organic structures but also paves the way for innovative applications in various fields.

Continued exploration of compounds like this could lead to significant advancements in chemistry and related disciplines, showcasing the beauty of molecular intricacies and their potential for real-world applications.

Synonyms
Forskolin Racemate
66428-89-5
(-)-Forskolin
1H-Naphtho[2,1-b]pyran-1-one,5-(acetyloxy)-3-ethenyldodecahydro-6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-
SR-01000075497
UPCMLD-DP135
Lopac0_000487
6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-3-vinyldodecahydro-1h-benzo[f]chromen-5-yl acetate
CHEMBL1358402
SCHEMBL14614874
UPCMLD-DP135:001
UPCMLD-DP135:002
CHEBI:93891
DTXSID00860823
HMS3261B15
64657-11-0
Tox21_500487
AKOS030228565
CCG-204578
LP00487
NCGC00015445-02
NCGC00015445-03
NCGC00015445-04
NCGC00015445-05
NCGC00093892-01
NCGC00161668-01
NCGC00162171-01
NCGC00261172-01
DB-054939
EU-0100487
F 6886
SR-01000075497-1
SR-01000075497-5
BRD-A70449690-001-01-4
Q27165646
(3R,6aalpha)-5alpha-Acetoxydodecahydro-6beta,10alpha,10balpha-trihydroxy-3,4abeta,7,7,10abeta-pentamethyl-3alpha-vinyl-1H-naphtho[2,1-b]pyran-1-one
1H-Naphtho[2, 5-(acetyloxy)-3-ethenyldodecahydro-6,10,10b-trihydroxy- 3,4a,7,7,10a-pentamethyl-, [3R-(3.alpha.,4a.beta., 5.beta.,6.beta.,6a.alpha.,10.alpha.,10a.beta.,10b.alpha.)]-
acetic acid (3-ethenyl-6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-5,6,6a,8,9,10-hexahydro-2H-benzo[f][1]benzopyran-5-yl) ester