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Tolterodine

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Identification
Molecular formula
C22H31N3O4S2
CAS number
124937-52-6
IUPAC name
4-methyl-N-[3-[3-(p-tolylsulfonylamino)propylamino]propyl]benzenesulfonamide
State
State

At room temperature, Tolterodine is typically found in a solid state.

Melting point (Celsius)
202.00
Melting point (Kelvin)
475.15
Boiling point (Celsius)
235.60
Boiling point (Kelvin)
508.75
General information
Molecular weight
475.63g/mol
Molar mass
475.6330g/mol
Density
1.2500g/cm3
Appearence

Tolterodine is a white to off-white crystalline powder.

Comment on solubility

Solubility of 4-methyl-N-[3-[3-(p-tolylsulfonylamino)propylamino]propyl]benzenesulfonamide

The solubility of 4-methyl-N-[3-[3-(p-tolylsulfonylamino)propylamino]propyl]benzenesulfonamide can be influenced by various factors due to its complex structure. Here are some points to consider:

  • Sulfonamide Group: The presence of the sulfonamide functional group generally enhances solubility in water due to the ability to form hydrogen bonds.
  • Amine Presence: The amino groups in the structure may contribute to increased polarity, enhancing solubility in polar solvents.
  • Hydrophobic Components: The presence of the p-tolyl group can introduce hydrophobic characteristics, which may limit solubility in aqueous environments.

"The balance between hydrophilic and hydrophobic components plays a critical role in determining the solubility of this compound."

Overall, while 4-methyl-N-[3-[3-(p-tolylsulfonylamino)propylamino]propyl]benzenesulfonamide is expected to have some degree of solubility in water, its precise solubility would need to be determined experimentally. Factors such as temperature, pH, and the presence of solvents could significantly affect the solubility behavior.

Interesting facts

Interesting Facts about 4-methyl-N-[3-[3-(p-tolylsulfonylamino)propylamino]propyl]benzenesulfonamide

This compound, a member of the sulfonamide class, presents a fascinating case of molecular complexity and therapeutic potential. Sulfonamides have been utilized extensively in medicinal chemistry due to their bacteriostatic properties. Here are some engaging points about this compound:

  • Molecular Functionality: The presence of sulfonamide functional groups allows this compound to interact with bacterial enzymes, inhibiting their growth and replication.
  • Versatile Applications: As a sulfonamide, it can serve various roles, from being a precursor in synthesis to functioning as a potential therapeutic agent targeting specific pathways in microbial infections.
  • Structure-Activity Relationships: The intricate structure, including the p-tolylsulfonylamino group, indicates a tailored design aimed at enhancing its biological activity and selectivity.
  • Advanced Research: Scientists are continually exploring the modifications of sulfonamide structures to improve efficacy and reduce side effects, showcasing the compound's evolving profile in pharmacology.

"Chemical innovation lies in the details of structure and synthesis," as one saying in the scientific community goes, emphasizing how compounds like this can lead to breakthroughs in treating resistant bacterial strains.

Overall, the study of 4-methyl-N-[3-[3-(p-tolylsulfonylamino)propylamino]propyl]benzenesulfonamide offers significant insight into the interplay between chemical structure and biological function, making it a vital compound for researchers in both organic and medicinal chemistry.