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Sodium salicylate

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Identification
Molecular formula
C7H5NNaO2
CAS number
54-21-7
IUPAC name
sodium;2-carbamoylphenolate
State
State

At room temperature, sodium salicylate exists as a solid.

Melting point (Celsius)
200.00
Melting point (Kelvin)
473.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
160.11g/mol
Molar mass
160.1060g/mol
Density
1.4457g/cm3
Appearence

Sodium salicylate is a white, crystalline solid that can appear in powder form. It is odorless and has a distinctly bitter and slightly saline taste.

Comment on solubility

Solubility of Sodium 2-Carbamoylphenolate

Sodium 2-carbamoylphenolate, a compound with notable chemical behavior, displays a significant degree of solubility in water. This is primarily due to the presence of the sodium ion, which increases the compound’s interaction with water molecules through ion-dipole interactions.

Several factors contribute to its solubility:

  • Polarity: The carbamoyl (-NH2) and phenolate (-O-) groups enhance the overall polarity of the molecule, making it more compatible with polar solvents like water.
  • Ion Formation: The dissociation into sodium ions (Na+) and 2-carbamoylphenolate ions in solution promotes solubility.
  • Hydrogen Bonding: The ability of the compound to engage in hydrogen bonding with water molecules further facilitates solubility.

This solubility characteristic is particularly significant in applications where the compound is utilized in aqueous environments. Thus, we can conclude that:

  1. The high solubility of sodium 2-carbamoylphenolate in water makes it an ideal candidate for various biochemical and analytical applications.
  2. It plays a crucial role in organic synthesis contexts where aqueous solutions are preferred.

Overall, sodium 2-carbamoylphenolate stands out in chemical environments due to its soluble nature, allowing for diverse usages and interactions with other chemical species.

Interesting facts

Interesting Facts about Sodium;2-Carbamoylphenolate

Sodium;2-carbamoylphenolate, often referred to as a sodium salt of 2-carbamoylphenol, is a fascinating compound with notable applications in various fields.

Chemical Insights

  • Structure and Stability: The compound features a phenol ring with a carbamoyl group, contributing to its chemical stability and reactivity. This structure allows for hydrogen bonding, influencing its solvation properties.
  • pH Influence: As a sodium salt, it often exhibits basic properties and can participate in acid-base reactions. This characteristic is particularly useful in various analytical chemistry applications, especially in titrations.
  • Biological Relevance: Compounds similar to sodium;2-carbamoylphenolate have been studied for their potential role as enzyme inhibitors and can play a part in biological systems, making them interesting in pharmacology and environmental science.

Applications

This compound is utilized in several areas:

  • Pharmaceutical Industry: It can serve as an intermediate in the synthesis of various drugs, offering a pathway for the development of novel therapeutics.
  • Analytical Chemistry: Sodium;2-carbamoylphenolate is often used as a reagent in qualitative and quantitative analyses due to its ability to form complexes with metal ions.
  • Research Applications: Studies exploring its role in organic synthesis continue to reveal intriguing pathways for developing new chemical entities.

Noteworthy Observations

  • Researchers often cite its versatility, with applications ranging from academia to industry.
  • Its resonance-stabilized structure is a highlight for students learning about aromatic compounds and their derivatives.
  • The interactions of this compound at different pH levels provide critical learning experiences regarding acid-base chemistry.

In summary, sodium;2-carbamoylphenolate is more than just a chemical; it embodies a bridge between theoretical concepts and practical applications, making it an exciting subject of study in the world of chemistry.