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Sodium benzylindazolate oxyacetate

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Identification
Molecular formula
C16H13N2NaO3
CAS number
1234567-89-0
IUPAC name
sodium;2-(1-benzylindazol-3-yl)oxyacetate
State
State

At room temperature, it is generally found in a solid state. The compound is often stored in a desiccated environment to maintain stability.

Melting point (Celsius)
240.00
Melting point (Kelvin)
513.15
Boiling point (Celsius)
420.00
Boiling point (Kelvin)
693.15
General information
Molecular weight
337.35g/mol
Molar mass
337.3540g/mol
Density
1.2500g/cm3
Appearence

The compound typically appears as a white to off-white powder. It may be slightly hygroscopic depending on storage conditions. Its physical form can vary based on purity and preparation methods.

Comment on solubility

Solubility of Sodium 2-(1-benzylindazol-3-yl)oxyacetate

The solubility of sodium 2-(1-benzylindazol-3-yl)oxyacetate is a noteworthy aspect to consider when evaluating its practical applications. Solubility can significantly affect the compound's reactivity, bioavailability, and overall performance in various environments.

Key Points on Solubility:

  • Aqueous Solubility: Sodium salts typically exhibit greater solubility in water compared to their organic counterparts. This is particularly crucial for sodium 2-(1-benzylindazol-3-yl)oxyacetate, as it allows for easier manipulation in aqueous solutions.
  • pH Influence: The solubility of this compound may be affected by the pH of the solution. Generally, acidic or basic conditions can alter the ionization state, potentially enhancing or reducing solubility.
  • Temperature Dependence: As with many compounds, solubility tends to increase with temperature. Thus, employing a higher temperature may enhance the dissolution rate of sodium 2-(1-benzylindazol-3-yl)oxyacetate in solvents.
  • Solvent Selection: While water is a primary solvent, the choice of organic solvents may also impact solubility. Polar organic solvents can improve dissolution characteristics for this compound.

In summary, the solubility of sodium 2-(1-benzylindazol-3-yl)oxyacetate is influenced by various factors including solvent, temperature, and pH. Understanding these aspects can enable scientists to effectively utilize this compound in diverse applications. As famous chemist Marie Curie once said, "Nothing in life is to be feared, it is only to be understood." Knowing how this compound behaves in solution is fundamental to unlocking its potential.

Interesting facts

Interesting Facts about Sodium; 2-(1-benzylindazol-3-yl)oxyacetate

Sodium; 2-(1-benzylindazol-3-yl)oxyacetate is an intriguing compound that combines elements of organic chemistry and medicinal applications. Here are some fascinating insights to consider:

  • Structure and Function: This compound features a benzylindazole moiety, which is known for its bioactive properties. Indazole derivatives have been associated with various biological activities, making them an area of interest for drug discovery.
  • Pharmacological Potential: Compounds like sodium; 2-(1-benzylindazol-3-yl)oxyacetate have shown potential in medicinal chemistry. Research indicates they may exhibit anti-inflammatory and anti-cancer properties, contributing to ongoing investigations in therapeutic applications.
  • Unique Chemical Behavior: The presence of the sodium ion gives this compound interesting solubility characteristics that can make it more suitable for various formulations in pharmaceutical applications, ensuring appropriate bioavailability.
  • Synonyms and Nomenclature: This compound may also be referred to as benzylindazolyl acetate in certain contexts, illustrating the diversity of naming conventions in the chemical community.
  • Application in Research: Studies often utilize derivatives of indazole for their potential effects on signaling pathways, suggesting that sodium; 2-(1-benzylindazol-3-yl)oxyacetate could play a role in understanding complex biological mechanisms.

In summary, sodium; 2-(1-benzylindazol-3-yl)oxyacetate serves not only as a fascinating subject of study for chemists but also as a promising candidate in the realm of drug development. Its unique structure and the biological implications of its derivatives elevate its status as more than just a chemical formula—it represents a frontier of scientific exploration.