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Identification
Molecular formula
C13H13N3O5S
CAS number
123456-78-9
IUPAC name
2-[(2-sulfooxyethylhydrazono)methyl]quinoline-4-carboxylic acid
State
State

This compound is typically found in a solid state at room temperature due to its melting point.

Melting point (Celsius)
240.00
Melting point (Kelvin)
513.15
Boiling point (Celsius)
475.00
Boiling point (Kelvin)
748.15
General information
Molecular weight
322.30g/mol
Molar mass
322.2960g/mol
Density
1.3900g/cm3
Appearence

The compound generally appears as a solid substance. The color and texture can vary depending on the specific sample and purity, but typically it may exist in a powder or crystalline form.

Comment on solubility

Solubility of 2-[(2-sulfooxyethylhydrazono)methyl]quinoline-4-carboxylic acid

This compound, 2-[(2-sulfooxyethylhydrazono)methyl]quinoline-4-carboxylic acid, exhibits unique solubility characteristics due to its complex molecular structure. Understanding its solubility plays a crucial role in various applications, from pharmaceutical formulation to chemical synthesis.


Factors Affecting Solubility

  • Polarity: The presence of sulfooxy and carboxylic acid functional groups enhances the polarity of this compound, promoting solubility in polar solvents like water.
  • Hydrogen Bonding: The ability of the compound to form hydrogen bonds with solvent molecules can significantly increase its solubility.
  • Temperature: Generally, solubility can increase with temperature for many compounds, so testing at various temperatures may provide further insights.

In general, it can be summarized that:

  • The compound is likely to be soluble in polar solvents, mainly due to its ionic and polar groups.
  • It may exhibit limited solubility in non-polar solvents, as structural hydrophilicity dominates.

Overall, the solubility profile of 2-[(2-sulfooxyethylhydrazono)methyl]quinoline-4-carboxylic acid is critical for its practical applications and necessitates careful consideration of the solvent environment for optimal use.

Interesting facts

Interesting Facts About 2-[(2-sulfooxyethylhydrazono)methyl]quinoline-4-carboxylic acid

2-[(2-sulfooxyethylhydrazono)methyl]quinoline-4-carboxylic acid, a fascinating organic compound, belongs to the quinoline family, which is notable for its diverse applications in various fields, such as pharmaceuticals, agrochemicals, and dyes. This compound is especially intriguing due to its unique structure and potential biochemical properties, which could pave the way for novel discoveries in medicinal chemistry.

Key Features

  • Versatile Structure: The presence of both a carboxylic acid and a sulfonate group makes it a candidate for various chemical reactions, enhancing its utility in synthetic organic chemistry.
  • Biological Potential: Compounds related to quinoline have been studied for their antimicrobial, anti-inflammatory, and antitumor activities, suggesting the possible therapeutic implications of this specific compound.
  • Hydrazone Functionality: The hydrazone bond in its structure is significant because hydrazones are often used in drug design for their unique properties that can affect the biological activity of compounds.

Furthermore, the potential applications of this compound extend beyond medicinal chemistry. It could be utilized in biochemical assays as a probe or in the synthesis of complex organic molecules due to its reactivity and stability. As research continues, the exploration of 2-[(2-sulfooxyethylhydrazono)methyl]quinoline-4-carboxylic acid could unveil new pathways and methodologies in the world of organic synthesis.

In summary, the exploration of this compound signifies the intersection of chemistry and biology, emphasizing the importance of chemical diversity in discovering innovative solutions for contemporary scientific challenges.

Synonyms
4-Quinolinecarboxylicacid, 2-[[2-[2-(sulfooxy)ethyl]hydrazinylidene]methyl]-
DTXSID70275061
2-[(2-sulfooxyethylhydrazinylidene)methyl]quinoline-4-carboxylic acid