Propyl 3-(2-sulfamoylphenyl)acrylate

Identification

Molecular formula

C₁₂H₁₅NO₄S

CAS number

638-58-4

IUPAC name

propyl 3-(2-sulfamoylphenyl)prop-2-enoate

State

At room temperature, propyl 3-(2-sulfamoylphenyl)acrylate is typically a liquid, although it can solidify upon cooling due to its melting point being slightly above room temperature.

Melting point (Celsius)

27.50

Melting point (Kelvin)

300.65

Boiling point (Celsius)

303.40

Boiling point (Kelvin)

576.55

General information

Molecular weight

261.31g/mol

Molar mass

261.3070g/mol

Density

1.1985g/cm³

Appearence

Propyl 3-(2-sulfamoylphenyl)acrylate typically appears as a colorless to pale-yellow liquid. Its appearance may vary slightly based on purity and specific preparation methods.

Comment on solubility

Solubility of Propyl 3-(2-sulfamoylphenyl)prop-2-enoate

The solubility of propyl 3-(2-sulfamoylphenyl)prop-2-enoate can be an intriguing topic for study due to its unique structural attributes. Here are some key points regarding its solubility:

Polar vs. Non-Polar Solubility: The presence of the sulfamoyl group gives the compound a degree of polarity, which influences its solubility profile in various solvents.
Solvent Compatibility: Typically, it is more soluble in polar solvents such as water and ethanol, compared to non-polar solvents like hexane. This is primarily due to hydrogen bonding capabilities with water molecules.
Temperature Effects: Solubility can often increase with temperature, making it essential to consider thermal conditions in practical applications.
pH Influence: Changes in pH can affect the ionization of the sulfamoyl group, consequently impacting solubility, especially in aqueous solutions.

In conclusion, understanding the solubility of ^{propyl 3-(2-sulfamoylphenyl)prop-2-enoate} requires consideration of its molecular structure, the nature of the solvent, and environmental conditions. As with many compounds, a comprehensive solubility study is essential for optimizing its use in various applications.

Interesting facts

Interesting Facts about Propyl 3-(2-sulfamoylphenyl)prop-2-enoate

Propyl 3-(2-sulfamoylphenyl)prop-2-enoate is a fascinating compound, notable for its specific functional groups and potential applications in various fields. Here are some captivating aspects of this compound:

Sulfamoyl Group: The presence of the sulfonamide group in this compound, characterized by a sulfur atom bonded to a nitrogen atom and a carbon skeleton, is significant in medicinal chemistry. Compounds containing ^{–SO₂NH₂} groups have shown *antibacterial* properties and are key in drug development.
Alkenoate Structure: The alkenoate part (prop-2-enoate) is vital for its reactivity and desired properties in polymerization and chemical synthesis processes. The double bond can participate in various reactions, increasing the compound's versatility in organic synthesis.
Potential Applications: This compound could be explored as a precursor for novel drug candidates or in the synthesis of advanced materials due to its unique reactivity. Research is ongoing regarding materials that could be derived from it in the fields of drug delivery systems or biocompatible polymers.
Structure-Activity Relationship (SAR): Analyzing the structure of propyl 3-(2-sulfamoylphenyl)prop-2-enoate offers insights into how modifications to its structure might enhance biological activity or reduce side effects, an essential process in pharmaceutical development.

In conclusion, propyl 3-(2-sulfamoylphenyl)prop-2-enoate stands out not just for its chemical structure but also for its *potential impact on various scientific fields*. Understanding such compounds can pave the way for future innovations in therapeutics and materials science.