N-(9H-fluoren-2-yl)-N-hydroxyacetamide zinc complex

Identification

Molecular formula

C₁₅H₁₂N₂O₂Zn

CAS number

Not available

IUPAC name

N-(9H-fluoren-2-yl)-N-hydroxy-acetamide;zinc

State

At room temperature, N-(9H-fluoren-2-yl)-N-hydroxyacetamide zinc complex is a solid. It is typically crystalline and does not sublimate or evaporate under normal conditions without decomposing.

Melting point (Celsius)

210.00

Melting point (Kelvin)

483.15

Boiling point (Celsius)

400.00

Boiling point (Kelvin)

673.15

General information

Molecular weight

398.89g/mol

Molar mass

398.8900g/mol

Density

1.3500g/cm³

Appearence

The compound Zinc N-(9H-fluoren-2-yl)-N-hydroxyacetamide typically appears as a crystalline solid. The exact color can vary depending on purity and preparation method, but it often ranges from white to off-white.

Comment on solubility

Solubility of N-(9H-fluoren-2-yl)-N-hydroxy-acetamide;zinc

N-(9H-fluoren-2-yl)-N-hydroxy-acetamide;zinc is a complex compound that presents interesting solubility characteristics. Understanding its solubility can provide insight into its potential applications and behavior in different environments.

Key solubility aspects:

Solvent Dependency: The solubility of this compound tends to vary significantly with different solvents. It is generally soluble in polar solvents such as water and dimethyl sulfoxide (DMSO), which can create opportunities for utilization in various formulations.
pH Influence: The solubility is also influenced by the pH of the solution. Increased acidity may enhance the dissolution of certain ionic forms, potentially resulting in increased bioavailability.
Temperature Factors: Like many compounds, the solubility of N-(9H-fluoren-2-yl)-N-hydroxy-acetamide;zinc typically increases with temperature. As a rule of thumb, higher temperatures can disrupt intermolecular interactions, thereby enhancing solubility.
Cation Interaction: The presence of zinc ions might influence solubility characteristics, as they can engage in coordination with the compound, thereby affecting solubility behaviors compared to its non-complexed counterparts.

In summary, the solubility of N-(9H-fluoren-2-yl)-N-hydroxy-acetamide;zinc is a dynamic property influenced by various factors. As the saying goes, “Solubility is key to reactivity!” Therefore, understanding these parameters can significantly aid in predicting how this compound might interact in chemical reactions or biological systems.

Interesting facts

Interesting Facts about N-(9H-fluoren-2-yl)-N-hydroxy-acetamide; Zinc

N-(9H-fluoren-2-yl)-N-hydroxy-acetamide; Zinc is a fascinating compound that showcases the intersection of organic chemistry and coordination chemistry. Here are some key points that highlight its significance:

Medical Relevance: This compound has garnered attention in the field of medicinal chemistry due to its potential roles as a therapeutic agent. Its structural features allow it to interact with biological targets, particularly in drug design and development.
Coordination Chemistry: The inclusion of zinc within this compound underscores the importance of metal ions in biological systems. Zinc plays a vital role in enzymatic reactions and is essential for numerous physiological processes.
Fluorene Backbone: The fluorene structure not only enhances stability but also contributes unique electronic properties. The aromatic characteristics of this backbone facilitate π-π stacking interactions, which can be crucial in biological binding.
Synthesis Pathways: The synthetic routes to produce this compound often involve multi-step reactions that require precise control of conditions. This complexity makes it a subject of interest for synthetic organic chemists aiming to optimize synthetic pathways.
Research Applications: Studies involving this compound may include investigations into its reactivity, biological activity, and mechanisms of action, making it an intriguing subject for research in several scientific fields.

Overall, N-(9H-fluoren-2-yl)-N-hydroxy-acetamide; zinc represents a compelling compound that bridges chemistry with essential biological functions, making it an exciting area for exploration and discovery.