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Fesoterodine

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Identification
Molecular formula
C26H37N3O4S
CAS number
286930-03-8
IUPAC name
N-[4-[1-[2-(6-methyl-2-pyridyl)ethyl]piperidine-4-carbonyl]phenyl]methanesulfonamide
State
State

At room temperature, Fesoterodine is typically in a solid state, appearing as a crystalline white to off-white powder.

Melting point (Celsius)
218.00
Melting point (Kelvin)
491.15
Boiling point (Celsius)
556.50
Boiling point (Kelvin)
829.65
General information
Molecular weight
527.68g/mol
Molar mass
527.6790g/mol
Density
1.2400g/cm3
Appearence

Fesoterodine is typically found in crystalline powder form. It appears as a white to off-white solid.

Comment on solubility

Solubility of N-[4-[1-[2-(6-methyl-2-pyridyl)ethyl]piperidine-4-carbonyl]phenyl]methanesulfonamide

The solubility of the compound N-[4-[1-[2-(6-methyl-2-pyridyl)ethyl]piperidine-4-carbonyl]phenyl]methanesulfonamide (C26H37N3O4S) can greatly affect its application in various fields, particularly in pharmaceuticals and chemical research. Here are a few critical points regarding its solubility:

  • Water Solubility: The presence of the methanesulfonamide functional group often enhances solubility in water, but the overall structure can lead to variable solubility results.
  • Solvent Compatibility: This compound may dissolve more readily in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), or acetonitrile rather than in pure water.
  • pH Dependence: Its solubility could be influenced by pH levels, with enhanced solubility in slightly acidic or basic conditions, depending on the ionization state of the molecule.
  • Temperature Influence: An increase in temperature may favor the solubility of this compound, making it more applicable in various reactions and formulations.

In conclusion, the solubility of N-[4-[1-[2-(6-methyl-2-pyridyl)ethyl]piperidine-4-carbonyl]phenyl]methanesulfonamide is crucial for understanding its bioavailability and effective utilization. As always, performing empirical measurements is recommended to obtain precise solubility data under specific conditions.

Interesting facts

Interesting Facts About N-[4-[1-[2-(6-methyl-2-pyridyl)ethyl]piperidine-4-carbonyl]phenyl]methanesulfonamide

N-[4-[1-[2-(6-methyl-2-pyridyl)ethyl]piperidine-4-carbonyl]phenyl]methanesulfonamide, colloquially referred to as a complex sulfonamide derivative, showcases remarkable structural diversity and potential in various scientific fields.

Chemical Structure and Functionality

  • Complex Architecture: The molecule comprises multiple functional groups, making it a potential candidate for various biological activities.
  • Biological Relevance: Sulfonamides are often associated with antimicrobial properties, highlighting the importance of this compound in medicinal chemistry.
  • Interaction Potential: The presence of a pyridine ring can enhance *lipophilicity* and *bioavailability*, which is crucial for drug design.

Applications in Research

  • Drug Development: This compound may serve as an optimized scaffold in the search for novel pharmaceutical agents.
  • Investigative Studies: Researchers can utilize it to explore *enzyme inhibition* and other mechanisms of action.
  • Collaboration with Biologists: By partnering with biologists, chemists can identify how this compound interacts with biological systems.

Why Study This Compound?

Studying N-[4-[1-[2-(6-methyl-2-pyridyl)ethyl]piperidine-4-carbonyl]phenyl]methanesulfonamide can be exceptionally enlightening for various reasons:

  • Understanding Structure-Activity Relationships (SAR): Delving into how different modifications can affect activity.
  • Integration of Multidisciplinary Approaches: Engaging in cross-disciplinary research can lead to innovative therapeutic solutions.

In conclusion, the intricate nature of this compound not only makes it interesting from a theoretical standpoint but also emphasizes its practical significance in the world of science and medicine. The exploration of such complex compounds can lead to groundbreaking discoveries that can impact various aspects of health and wellness.

Synonyms
113558-89-7
E-4031
E 4031
N-[4-[1-[2-(6-methylpyridin-2-yl)ethyl]piperidine-4-carbonyl]phenyl]methanesulfonamide
E4031
1L1K8X5DF9
2-Methyl-6-(2-(4-(4-methylsulfonylamino)benzoylpiperidin-1-yl)ethyl)pyridine
UNII-1L1K8X5DF9
N-(4-((1-(2-(6-Methyl-2-pyridinyl)ethyl)-4-piperidinyl)carbonyl)phenyl)methanesulfonamide
CHEMBL327980
CHEBI:34732
DTXSID00150458
Methanesulfonamide, N-(4-((1-(2-(6-methyl-2-pyridinyl)ethyl)-4-piperidinyl)carbonyl)phenyl)-
N-[4-[[1-[2-(6-methyl-2-pyridinyl)ethyl]-4-piperidinyl]carbonyl]phenyl]methanesulfonamide dihydrochloride
N-[4-[1-[2-(6-methyl-2-pyridyl)ethyl]piperidine-4-carbonyl]phenyl]methanesulfonamide
N-(4-(1-(2-(6-methyl-2-pyridyl)ethyl)piperidine-4-carbonyl)phenyl)methanesulfonamide
N-(4-(1-(2-(6-methylpyridin-2-yl)ethyl)piperidine-4-carbonyl)phenyl)methanesulfonamide
n-[4-[[1-[2-(6-methyl-2-pyridinyl)ethyl]-4-piperidinyl]carbonyl]phenyl]methanesulfonamide
Tocris-1808
A1L2J
BSPBio_001313
KBioGR_000033
KBioSS_000033
E-4031 FREE BASE
GTPL2605
SCHEMBL2168557
DTXCID9072949
KBio2_000033
KBio2_002601
KBio2_005169
KBio3_000065
KBio3_000066
Bio1_000373
Bio1_000862
Bio1_001351
Bio2_000033
Bio2_000513
HMS1791B15
HMS1989B15
HMS3402B15
BDBM50117930
IDI1_033783
NCGC00025301-01
NCGC00025301-02
NCGC00025301-03
NCGC00025301-04
AS-85254
G92486
Q5321366
BRD-K41713976-001-02-0
BRD-K41713976-300-01-8
BRD-K41713976-300-02-6
(4-{1-[2-(6-Methyl-pyridin-2-yl)-ethyl]-piperidine-4-carbonyl}-phenyl)-methanesulfonamide
1-(2-(6-methylpyridin-2-yl)ethyl)-4-(4-(methylsulfonamido)benzoyl)piperidinium
1-[2-(6-methyl-2-pyridyl)ethyl]-4-(4-methylsulfonyl-aminobenzoyl)piperidine
690-710-2
N-(2-{1-[2-(6-Methyl-pyridin-2-yl)-ethyl]-piperidine-4-carbonyl}-phenyl)-methanesulfonamide
N-(4-{1-[2-(6-Methyl-pyridin-2-yl)-ethyl]-piperidine-4-carbonyl}-phenyl)-methanesulfonamide
N-(4-{1-[2-(6-Methyl-pyridin-2-yl)-ethyl]-piperidine-4-carbonyl}-phenyl)-methanesulfonamide (E-4031)
N-[4-[[1-[2-(6-METHYL-2-PYRIDINYL)ETHYL]-4-PIPERIDINYL]CARBONYL]PHENYL]METHANESULFONAMIDE DIHYDROCHL