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Cruzain Inhibitor

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Identification
Molecular formula
C30H38N2O3
CAS number
133343-34-1
IUPAC name
2-hydroxy-2-oxo-acetate;2-(1-naphthyl)pent-4-enyl-(2-piperidin-1-ium-1-ylethyl)ammonium
State
State

At room temperature, it is typically a solid with a stable form suitable for handling under standard laboratory conditions.

Melting point (Celsius)
152.00
Melting point (Kelvin)
425.00
Boiling point (Celsius)
313.00
Boiling point (Kelvin)
586.00
General information
Molecular weight
499.65g/mol
Molar mass
499.6540g/mol
Density
1.2174g/cm3
Appearence

It appears as a powder or solid with a crystalline structure. The color can vary depending on purity and form, being typically white to off-white.

Comment on solubility

Solubility of 2-hydroxy-2-oxo-acetate; 2-(1-naphthyl)pent-4-enyl-(2-piperidin-1-ium-1-ylethyl)ammonium

The solubility of the compound 2-hydroxy-2-oxo-acetate; 2-(1-naphthyl)pent-4-enyl-(2-piperidin-1-ium-1-ylethyl)ammonium can be influenced by various factors due to its complex structure and multiple functional groups. When considering its solubility, several key points arise:

  • Polarity: The presence of polar functional groups, such as the hydroxyl and ammonium groups, suggests that this compound may exhibit decent solubility in polar solvents like water.
  • Hydrophobic Character: The naphthyl and pentenyl moieties contribute significant hydrophobic character, which might limit solubility in water but enhance it in non-polar organic solvents.
  • pH Dependency: Being an ammonium salt, the solubility could vary with changes in pH, with increased solubility in acidic conditions where the ammonium form predominates.
  • Temperature Effects: Elevated temperatures frequently increase solubility, thus the compound’s solubility might improve when heated.

In conclusion, while the exact solubility can depend on the specific conditions, it is likely that the compound is soluble in a range of solvents, especially those that accommodate both its hydrophilic and hydrophobic regions. As the famous saying goes, "Like dissolves like," which aptly reflects the solubility behavior of this intriguing compound.

Interesting facts

Discovering 2-hydroxy-2-oxo-acetate; 2-(1-naphthyl)pent-4-enyl-(2-piperidin-1-ium-1-ylethyl)ammonium

This intriguing compound, known for its complex structure and unique properties, has become a subject of interest among chemists. Here are some captivating facts that highlight its significance:

  • Dual Character: The presence of both a hydroxy group and a piperidinium ion in the compound gives it both polar and nonpolar characteristics, making it versatile in many chemical reactions.
  • Biological Relevance: Compounds with similar structures are often researched for their potential biological activities, such as antimicrobial and anti-inflammatory properties. This opens doors to medicinal chemistry and therapeutic applications.
  • Reaction Mechanisms: The structure suggests a possible involvement in various reaction mechanisms, particularly in nucleophilic substitution and electrophilic addition reactions, which can be exciting for organic synthesis.
  • Pharmaceutical Applications: Given its complexity, this compound has potential as a lead structure in drug development. Researchers may explore its efficacy in targeting specific biological pathways.
  • Research Frontiers: Chemistry students and scientists are encouraged to dive into this compound for its potential implications in creating new materials and pharmaceuticals. As one researcher aptly put it, "Complexity breeds innovation."

Overall, 2-hydroxy-2-oxo-acetate; 2-(1-naphthyl)pent-4-enyl-(2-piperidin-1-ium-1-ylethyl)ammonium serves as a remarkable example of how intricate chemical structures can lead to profound discoveries and breakthroughs in science.

Synonyms
4-Pentenylamine, 2-(1-naphthyl)-N-(2-piperidinoethyl)-, bioxalate
10337-43-6
N-(2-Piperidinoethyl)-beta-(2-propenyl)-1-naphthaleneethylamine bioxalate
1-NAPHTHALENEETHYLAMINE, N-(2-PIPERIDINOETHYL)-beta-(2-PROPENYL)-, BIOXALATE