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Abiemic Acid

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Identification
Molecular formula
C27H40O7
CAS number
146052-83-7
IUPAC name
5-[14-hydroxy-10,13-dimethyl-3-(3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl)oxy-1,2,3,6,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]pyran-2-one
State
State

At room temperature, Abiemic Acid is in solid state. It is stable and maintains structural integrity under standard conditions.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
452.62g/mol
Molar mass
452.6230g/mol
Density
1.2800g/cm3
Appearence

Abiemic Acid typically appears as a white to off-white crystalline solid. Its structure is a complex polycyclic hydrocarbon with multiple hydroxyl groups, giving it a slightly waxy texture.

Comment on solubility

Solubility of 5-[14-hydroxy-10,13-dimethyl-3-(3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl)oxy-1,2,3,6,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]pyran-2-one

The solubility of the compound with the chemical formula C27H40O7 can be influenced by several factors due to its complex structure. Here are some key points to consider:

  • Polarity: This compound contains multiple hydroxyl groups, which may increase its polar character, enhancing solubility in polar solvents like water.
  • Hydrophilicity: The presence of trihydroxy groups suggests a potential for strong interactions with water molecules, leading to improved solubility.
  • Hydrophobic Regions: However, the large hydrophobic hydrocarbon portions may limit solubility in highly polar solvents.
  • Solvent Interactions: It may exhibit varying solubility in organic solvents such as ethanol or methanol, which can better accommodate both polar and nonpolar elements of the molecule.

In summary, while this compound may demonstrate notable solubility in polar solvents due to its hydroxy groups, its overall solubility profile is likely to be complex, necessitating careful consideration of both its hydrophilic and hydrophobic characteristics. Ultimately, the solubility of such a multifaceted molecule emphasizes the importance of understanding the interplay between its structural features and solvent properties.

Interesting facts

Interesting Facts about 5-[14-hydroxy-10,13-dimethyl-3-(3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl)oxy-1,2,3,6,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]pyran-2-one

This complex compound, known for its multifaceted structure, is a fascinating example of organic chemistry. Here are some captivating insights:

  • Biological Significance: Compounds like this one often exhibit biological activity, making them potential candidates for pharmacological applications. Their intricate structures can influence their interactions within biological systems.
  • Synthetic Challenges: The synthesis of such a polycyclic structure can be quite challenging. Chemists must skillfully navigate several steps, including functional group transformations and stereochemical considerations.
  • Natural Boundaries: Many compounds with similar structural motifs are found in nature, particularly in plants. Investigating these compounds may reveal insights into their roles in nature, such as defense mechanisms or ecological interactions.
  • Applications in Medicine: Given the presence of hydroxyl functional groups, this compound may have applications in drug design, particularly in developing agents that target specific enzymes or receptors in the human body.
  • Research Thrills: Scientists continue to uncover new information regarding such compounds, which can lead to breakthroughs in medicinal chemistry and material science.

As a chemistry student or researcher, exploring the properties and applications of compounds like this can open a window into understanding complex biochemical processes, and can even inspire the next significant innovation in drug development. As Albert Einstein once said, "Imagination is more important than knowledge." This is especially true in the realm of chemistry, where creativity and scientific understanding unite to unlock the mysteries of nature.

Synonyms
Proscillaridin A
Cardiovite
Proscillan
Proslladin
Sandoscill
Scillacrist
Caradrin
Caradrine
Cardion
Carmazon
Coratol
Procardin
Procilan
Prostosin
Proszin
Protasin
Solestril
Stellarid
Tradenal
Urgilan
Wirnesin
Simeon
Herzo proscillan
Purosin-TC
Transvaalin, degluco-
PSC-801
Desglucotransvaaline
A-32686
Scillarenin 3.beta.-rhamnoside
Proszine
Desglucotrnasvaaline
Scillarenin, 3.alpha.-L-rhamnopyranoside
Scilla ''didier''
MYEJFUXQJGHEQK-UHFFFAOYSA-N
AKOS030255146
5-[11-hydroxy-2,15-dimethyl-5-(3,4,5-trihydroxy-6-methyl(2H-3,4,5,6-tetrahydro pyran-2-yloxy))tetracyclo[8.7.0.0<2,7>.0<11,15>]heptadec-6-en-14-yl]pyran-2-on e
Rhamnopyranoside, scillarenin-3, .alpha.-L-
14-Hydroxy-3.beta.-(rhamnosyloxy)bufa-4,20,22-trienolide
3-.beta.,14-.beta.-Dihydroxybufa-4,20,22-trienolide 3-rhamnoside
3.beta.,14.beta.-dihydroxybufa-4,20,22-trienolide 3-rhamnoside
3.beta.-Rhamnosido-14.beta.-hydroxy-.DELTA.4,20,22-bufatrienolide
3-.beta.-((6-Deoxy-.alpha.-L-mannopyranosyl)oxy)-14-hydroxybufa-4,20,22-trienolide
3.beta.-[(6-Deoxy-.alpha.-L-mannopyranosyl)oxy]-14-hydroxybufa-4,20,22-trienolide
Bufa-4,20,22-trienolide, 3-.beta.-((6-deoxy-.alpha.-L-mannosyl)oxy)-14-hydroxy-
Bufa-4,20,22-trienolide, 3.beta.-((6-deoxy-.alpha.-L-mannopyranosyl)oxy)-14-hydroxy-
Bufa-4,20,22-trienolide, 3.beta.-((6-deoxy-.alpha.-L-mannosyl)oxy)-14-hydroxy-