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D-Boronoprolíne

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Identification
Molecular formula
C5H11BN2O4
CAS number
1637-08-1
IUPAC name
(5-amino-5-carboxy-pentyl)-trihydroxy-boranuide
State
State

Solid at room temperature.

Melting point (Celsius)
202.00
Melting point (Kelvin)
475.15
Boiling point (Celsius)
349.92
Boiling point (Kelvin)
623.07
General information
Molecular weight
208.02g/mol
Molar mass
208.0190g/mol
Density
1.2170g/cm3
Appearence

White crystalline solid.

Comment on solubility

Solubility of (5-amino-5-carboxy-pentyl)-trihydroxy-boranuide (C5H11BN2O4)

The solubility of (5-amino-5-carboxy-pentyl)-trihydroxy-boranuide is an intriguing topic due to its unique chemical structure. Several factors influence its solubility characteristics, which can be summarized as follows:

  • Polarity: The presence of multiple functional groups such as amino (-NH2), carboxy (-COOH), and hydroxyl (-OH) enhances the polarity of this compound.
  • Hydrogen bonding: The -NH2 and -OH groups can form hydrogen bonds with water molecules, suggesting increased solubility in polar solvents.
  • Ionic interactions: The carboxylic group can ionize in aqueous solutions, further facilitating solubility through ionic interactions.
  • Solvent effects: Based on the solvent used, solubility may vary significantly. For example, it is likely to be more soluble in water compared to non-polar organic solvents.

Overall, one might summarize the solubility behavior of this compound as generally favorable in polar solvents, particularly water, due to its capacity to engage in hydrogen bonding and ionic interactions. However, exact solubility values may vary and experimental data would provide the most accurate insights.

Interesting facts

Interesting Facts about (5-amino-5-carboxy-pentyl)-trihydroxy-boranuide

(5-amino-5-carboxy-pentyl)-trihydroxy-boranuide is a fascinating compound that has captured the attention of researchers in various fields. Here are several intriguing aspects of this compound:

  • Unique Structure: This compound features both amino and carboxyl functional groups, making it an important building block in organic synthesis and medicinal chemistry.
  • Borane Chemistry: The presence of boron in its structure hints at the study of boron chemistry, known for its applications in pharmaceuticals and materials science.
  • Hydroxy Groups: With three hydroxy groups, this compound exhibits potential as a chelating agent, which can bind to metal ions effectively.
  • Biological Relevance: The amino and carboxyl groups suggest that (5-amino-5-carboxy-pentyl)-trihydroxy-boranuide can play a role in biochemical pathways, possibly affecting nitrogen metabolism.
  • Research Opportunities: The complexity of its structure offers rich interactions for further studies, including its potential therapeutic uses in targeting specific biological pathways.

Applications and Future Research

Ongoing research on this compound could lead to significant discoveries in multiple domains:

  • Potential applications in drug design, especially involving bioconjugation.
  • Investigations into its role as a boron carrier in cancer therapy.
  • Exploration of its properties as a biodegradable material in environmental chemistry.

In summary, (5-amino-5-carboxy-pentyl)-trihydroxy-boranuide is a testament to the interplay of diverse chemical functionalities, opening avenues for multidisciplinary research and innovation. As we continue to unravel the mysteries surrounding such compounds, we may find solutions to some of today's most pressing challenges in chemistry and beyond.

Synonyms
PD042828