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Abietic Acid Acetate

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Identification
Molecular formula
C22H34O4
CAS number
481-54-5
IUPAC name
[(3R,4R,6S,8S,9R,10R,14R,16R)-3,4,6,9,14-pentahydroxy-5,5,9,14-tetramethyl-16-tetracyclo[11.2.1.01,10.04,8]hexadecanyl] acetate
State
State

At room temperature, Abietic Acid Acetate is typically in a solid state.

Melting point (Celsius)
146.00
Melting point (Kelvin)
419.15
Boiling point (Celsius)
200.00
Boiling point (Kelvin)
473.15
General information
Molecular weight
358.49g/mol
Molar mass
358.4880g/mol
Density
1.0645g/cm3
Appearence

Abietic Acid Acetate appears as a white crystalline solid. It has a distinctive, resinous odor.

Comment on solubility

Solubility of the Compound

The solubility of the compound [(3R,4R,6S,8S,9R,10R,14R,16R)-3,4,6,9,14-pentahydroxy-5,5,9,14-tetramethyl-16-tetracyclo[11.2.1.01,10.04,8]hexadecanyl] acetate can be quite intriguing due to its complex structural configuration.

Based on the presence of various functional groups and steric factors, solubility behavior can be analyzed through the following aspects:

  • Hydroxyl Groups: The compound features multiple hydroxyl (-OH) groups, which generally enhance solubility in polar solvents such as water.
  • Hydrophobic Regions: The presence of tetracyclic systems and bulky hydrocarbon chains may contribute to hydrophobic characteristics, resulting in limited solubility in non-polar solvents.
  • Overall Solubility: The balance between the hydrophilic -OH groups and the hydrophobic portions determines its combined solubility profile.

Thus, the solubility of this compound can be described as moderate in polar solvents, while it may exhibit lower solubility in non-polar mediums. Understanding these properties can significantly aid in the applications of this compound in various chemical processes.

Interesting facts

Interesting Facts About the Compound

This fascinating compound is a member of the steroid family and possesses a complex structure that makes it a subject of significant interest in both synthetic and natural product chemistry.

Key Characteristics

  • Stereochemistry: The specific stereochemical configuration, denoted by its extensive (R/S) notation, suggests that this compound can exhibit unique biological activities due to its three-dimensional shape. This stereochemistry plays a crucial role in how the molecule interacts with biological targets.
  • Natural Sources: Compounds with similar frameworks are often found in various natural sources, including plants and fungi. They can be vital to ecological interactions, such as providing defense against herbivores or acting as signaling molecules.
  • Chemical Modifications: The acetylation observed in this compound showcases the ability of chemists to modify natural substances to enhance their stability or bioavailability. Such modifications can lead to compounds with improved pharmacological properties.
  • Potential Applications: Due to its structure, this compound may have applications in pharmaceuticals or cosmetic formulations. Compounds with similar backbones are frequently studied for their anti-inflammatory, anti-cancer, and antimicrobial properties.

Relevance in Research

As researchers continue to explore the universe of chemical structures, compounds like this one hold promises that extend beyond academia. They push the boundaries of drug discovery, natural product extraction, and even synthetic organic chemistry approaches. As one recent study observed, "understanding the intricate architecture of such compounds can reveal untapped potential for new therapeutic agents."

In summary, the intricate structure and potential applications of this compound make it a noteworthy subject of investigation in the vast field of chemistry. Every aspect of its chemistry invites scientists to deepen their understanding and explore the diverse possibilities that stems from nature’s designs.

Synonyms
Spectrum_000240
SpecPlus_000225
Spectrum2_000557
Spectrum3_000232
Spectrum4_001529
Spectrum5_000038
BSPBio_001903
KBioGR_001938
KBioSS_000720
SPECTRUM201662
DivK1c_006321
SPBio_000633
KBio1_001265
KBio2_000720
KBio2_003288
KBio2_005856
KBio3_001403
CCG-38725
NCGC00178915-01
PD118961
SR-05000002651
SR-05000002651-1