N,N-diethyl-3-methyl-2-(p-tolylsulfonylamino)butanamide

Identification

Molecular formula

C₁₆H₂₅NO₃S

CAS number

5537-17-7

IUPAC name

N,N-diethyl-3-methyl-2-(p-tolylsulfonylamino)butanamide

State

At room temperature, N,N-diethyl-3-methyl-2-(p-tolylsulfonylamino)butanamide is a solid. It maintains stability in this form under standard atmospheric conditions.

Melting point (Celsius)

98.50

Melting point (Kelvin)

371.65

Boiling point (Celsius)

465.50

Boiling point (Kelvin)

738.65

General information

Molecular weight

316.42g/mol

Molar mass

316.4230g/mol

Density

1.1540g/cm³

Appearence

N,N-diethyl-3-methyl-2-(p-tolylsulfonylamino)butanamide typically appears as a white crystalline solid. The purity can affect the exact shade and form of the crystals. It is generally devoid of any distinct color if highly pure.

Comment on solubility

Solubility of N,N-Diethyl-3-methyl-2-(p-tolylsulfonylamino)butanamide

The solubility of N,N-diethyl-3-methyl-2-(p-tolylsulfonylamino)butanamide (C₁₆H₂₅NO₃S) can be described with several important considerations:

Polarity: The compound has both polar and nonpolar characteristics due to its amide and sulfonyl groups combined with alkyl chains. This dual nature significantly influences its solubility in different solvents.
Solvent Compatibility: Typically, compounds similar to this one tend to be more soluble in polar aprotic solvents like DMSO or DMF, while showing limited solubility in nonpolar solvents.
Hydrogen Bonding: The presence of functional groups capable of hydrogen bonding can increase solubility in water, although the overall structure might still pose challenges.
Temperature Effects: Solubility could improve at elevated temperatures, as increased kinetic energy often helps dissolve more solute in a solvent.

In conclusion, while the exact solubility parameters depend on specific conditions, it's essential to consider factors such as polarity, solvent choice, and temperature when evaluating the solubility of this complex molecule. As with many organic compounds, comprehensive solubility data may necessitate experimental determination to draw definitive conclusions.

Interesting facts

N,N-Diethyl-3-methyl-2-(p-tolylsulfonylamino)butanamide

N,N-diethyl-3-methyl-2-(p-tolylsulfonylamino)butanamide is a fascinating compound with a diverse range of applications and intriguing characteristics. Here are some interesting facts to consider:

Pharmaceutical Applications: This compound plays a significant role in medicinal chemistry due to its structure, which allows it to interact with biological systems effectively. It is often studied for its potential therapeutic effects.
Structure and Function: The unique combination of the diethyl and p-tolyl groups contributes to the compound's properties. The sulfonamide group specifically enhances the molecule’s reactivity and ability to bind to enzymes, which is vital for its biological activity.
Mechanism of Action: Research indicates that compounds like N,N-diethyl-3-methyl-2-(p-tolylsulfonylamino)butanamide may exert their effects through modulation of specific receptors or enzymes, making them of great interest to scientists focused on drug design.
Research Potential: Ongoing studies into this compound could lead to the discovery of new therapeutic agents, especially in combating diseases where traditional treatments fail. As such, its synthesis and mechanism are active areas of research in the field of medicinal chemistry.

In summary, N,N-diethyl-3-methyl-2-(p-tolylsulfonylamino)butanamide exemplifies the intersection of organic chemistry and pharmacology. With its structurally intricate design and potential medical relevance, it remains a subject of significant scientific intrigue.

Synonyms

AKOS024342489

N,N-DIETHYL-3-METHYL-2-(TOLUENE-4-SULFONYLAMINO)-BUTYRAMIDE