Skip to main content

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

ADVERTISEMENT
Identification
Molecular formula
C13H17NO4S
CAS number
154417-63-1
IUPAC name
butyl 3-(2-sulfamoylphenyl)prop-2-enoate
State
State

At room temperature, Butyl 3-(2-sulfamoylphenyl)prop-2-enoate is primarily found in a solid state.

Melting point (Celsius)
100.20
Melting point (Kelvin)
373.35
Boiling point (Celsius)
375.20
Boiling point (Kelvin)
648.35
General information
Molecular weight
271.32g/mol
Molar mass
271.3230g/mol
Density
1.2380g/cm3
Appearence

Butyl 3-(2-sulfamoylphenyl)prop-2-enoate typically appears as a white to off-white crystalline powder. It may also be encountered as a solid or solidified liquid, depending on the conditions of storage and handling.

Comment on solubility

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

butyl 3-(2-sulfamoylphenyl)prop-2-enoate, a compound known for its intriguing properties, demonstrates varying levels of solubility depending on the solvent used. Generally, the solubility can be summarized as follows:

  • Polar solvents: The presence of the sulfamoyl group typically enhances solubility in polar solvents such as water and alcohols due to strong hydrogen bonding.
  • Non-polar solvents: Conversely, in non-polar solvents like hexane or toluene, the compound exhibits lower solubility owing to poor interactions.
  • pH Sensitivity: The solubility may also vary with pH levels, significantly increasing in alkaline conditions due to deprotonation of the sulfamoyl group.

As a rule of thumb, the effectiveness of a solvent can often be assessed by considering the principle of "like dissolves like," where similar polarity between solute and solvent typically leads to better solubility. In practical applications, thorough testing is advised to identify the most effective solvent for dissolving butyl 3-(2-sulfamoylphenyl)prop-2-enoate.

Interesting facts

Exploring Butyl 3-(2-sulfamoylphenyl)prop-2-enoate

Butyl 3-(2-sulfamoylphenyl)prop-2-enoate is a fascinating compound that blends organic and medicinal chemistry, showcasing the versatility of sulfonamide derivatives. This compound has attracted interest due to its potential applications in pharmaceuticals, particularly as it relates to anti-inflammatory and antibacterial activities.

Key Features of Butyl 3-(2-sulfamoylphenyl)prop-2-enoate

  • Structure Complexity: The integration of a sulfamoyl group into the phenyl ring enhances the compound's reactivity and biological activity, making it a valuable subject for drug design.
  • Synthetic Pathways: Synthesizing this compound involves several intricate steps, often leveraging methods such as nucleophilic substitution or coupling reactions, illustrating the creativity required in synthetic chemistry.
  • Biological Potential: Preliminary studies suggest that this compound may offer therapeutic benefits due to its structural similarity to well-known sulfonamide antibiotics, prompting ongoing research into its efficacy.
  • Interdisciplinary Applications: Beyond pharmaceuticals, this compound might find applications in agricultural chemistry as a potential pesticide or herbicide, responding to the need for sustainable agricultural practices.

As a chemical scientist or student, delving into the properties and applications of butyl 3-(2-sulfamoylphenyl)prop-2-enoate offers an opportunity to appreciate the intersection of chemistry and real-world applications. Engaging with such compounds not only enhances our understanding of chemical reactivity but also piques our curiosity about their roles in improving health and industry.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." The study of this compound embodies this philosophy, challenging us to explore and innovate continuously in the field of chemistry!