Skip to main content

4-ethylsulfonylnaphthalene-1-sulfonamide

ADVERTISEMENT
Identification
Molecular formula
C12H13NO4S2
CAS number
17321-77-6
IUPAC name
4-ethylsulfonylnaphthalene-1-sulfonamide
State
State

At room temperature, the compound is in a solid state. It is typically stable under normal conditions of use and storage.

Melting point (Celsius)
163.00
Melting point (Kelvin)
436.15
Boiling point (Celsius)
395.00
Boiling point (Kelvin)
668.15
General information
Molecular weight
305.37g/mol
Molar mass
305.3680g/mol
Density
1.4200g/cm3
Appearence

4-Ethylsulfonylnaphthalene-1-sulfonamide is typically a white to off-white crystalline powder. Its appearance can vary depending on the purity and particle size.

Comment on solubility

Solubility of 4-ethylsulfonylnaphthalene-1-sulfonamide

4-ethylsulfonylnaphthalene-1-sulfonamide is an intriguing compound, particularly when it comes to its solubility properties. Understanding its solubility can provide insights into its potential applications in various fields.

Key Factors Affecting Solubility

The solubility of this compound can be influenced by several factors:

  • Polarity: The presence of sulfonamide and sulfonyl groups contributes to its polarity, which often enhances solubility in polar solvents.
  • Hydrogen Bonding: The ability of sulfonamide groups to participate in hydrogen bonding can lead to increased solubility in water.
  • Molecular Size: The larger molecular structure can cause decreased solubility in non-polar solvents.

Solvent Compatibility

When considering solvents, it is essential to highlight:

  • Water: Likely to exhibit reasonable solubility due to its polar nature.
  • Alcohols: Such as ethanol may dissolve the compound effectively due to similar interactions.
  • Acetone: A good solvent option due to its ability to interact with the compound's functional groups.

In contrast, non-polar solvents such as hexane may not solubilize 4-ethylsulfonylnaphthalene-1-sulfonamide effectively, emphasizing the importance of solvent selection for desired applications.

In summary, understanding the solubility of 4-ethylsulfonylnaphthalene-1-sulfonamide is vital for its practical use, guiding researchers in selecting appropriate solvents for experiments and applications.

Interesting facts

Exploring 4-Ethylsulfonylnaphthalene-1-sulfonamide

4-Ethylsulfonylnaphthalene-1-sulfonamide is a fascinating compound that deserves attention for its unique structural and functional characteristics within the realm of chemistry.

Chemical Structure and Characteristics

  • Structural Complexity: This compound features a naphthalene backbone, which is well-known for its stability and aromatic character, combined with sulfonamide functionalities that impart distinctive chemical properties.
  • Functional Groups: The presence of both sulfonyl and sulfonamide groups in its structure not only influences reactivity but also grants the molecule potential applications in medicinal chemistry.

Applications and Significance

4-Ethylsulfonylnaphthalene-1-sulfonamide is not just a curiosity in the lab; it holds promise in various applications, including:

  • Pharmaceuticals: Compounds with sulfonamide structures have been pivotal in the development of various antibiotics and treatments for bacterial infections.
  • Research: This compound can serve as a valuable tool in biochemical research settings, providing insights into molecular interactions and enzyme inhibition.

Key Insights

As a student or scientist, it can be enlightening to ponder the synthesis routes of 4-Ethylsulfonylnaphthalene-1-sulfonamide. Many synthetic strategies integrate sulfonation methods, reflecting the versatility of sulfur chemistry. Remember, as Richard Feynman once emphasized, "The most useful thing about a principle is that it enables you to make predictions." Understanding the principles behind the synthesis and reactivity of such compounds can open doors to novel discoveries.

In conclusion, 4-Ethylsulfonylnaphthalene-1-sulfonamide is more than just a chemical entity. It embodies the intersection of structure, function, and application in chemistry, stimulating curiosity and encouraging further exploration.

Synonyms
4-Ethylsulfonylnaphthalene-1-sulfonamide
CCRIS 1566
4-Ethylsulphonylnaphthalene-1-sulfonamide
4-Ethylsulphonylnaphthalene-1-sulphonamide
4-(Ethylsulfonyl)-1-naphthalenesulfonamide
BRN 2153432
1-NAPHTHALENESULFONAMIDE, 4-(ETHYLSULFONYL)-
DTXSID9020613
4-11-00-00615 (Beilstein Handbook Reference)
DTXCID70613
842-00-2
4-(ethylsulfonyl)naphthalene-1-sulfonamide
4-Ethylsulfonylnaphthanele-1-sulfonamide
RZF8EV6BVY
SCHEMBL18889781
Ethylsulphonylnaphthalene-1-sulfonamide, 4-
Q63088207