Skip to main content

Org227222

ADVERTISEMENT
Identification
Molecular formula
C15H21IN2O3
CAS number
81938-24-1
IUPAC name
N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-3-iodo-6-methoxy-benzamide
State
State

At room temperature, the compound is a solid. It is generally stable under normal conditions but should be kept in a dry and cool environment to maintain its integrity.

Melting point (Celsius)
283.00
Melting point (Kelvin)
556.15
Boiling point (Celsius)
422.00
Boiling point (Kelvin)
695.15
General information
Molecular weight
405.23g/mol
Molar mass
405.2310g/mol
Density
1.6000g/cm3
Appearence

The compound typically appears as an off-white to pale yellow powder. It may be slightly hygroscopic depending on its formulation and surrounding humidity.

Comment on solubility

Solubility of N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-3-iodo-6-methoxy-benzamide

The solubility of N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-3-iodo-6-methoxy-benzamide (C15H21IN2O3) is quite intricate due to its unique structural characteristics.

Some key factors influencing its solubility include:

  • Polarity: The presence of hydroxyl (-OH) and methoxy (-OCH3) groups indicates potential for hydrogen bonding, which can enhance solubility in polar solvents.
  • Appendages: The ethyl-pyrrolidine moiety introduces a degree of hydrophobicity, suggesting that its solubility may be limited in highly polar solvents.
  • Iodine presence: The iodine atom may affect the overall solubility behavior, as halogens can add to the complexity of solvation dynamics.

For practical purposes, it is reasonable to expect that:

  1. This compound may display higher solubility in alcohols and dimethyl sulfoxide (DMSO) due to their ability to stabilize interactions with the polar functional groups.
  2. Conversely, it may be less soluble in non-polar solvents like hexane, given the hydrophilic nature imparted by the hydroxyl group.

In conclusion, while precise solubility data may vary, understanding these structural influences can guide predictions about N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-3-iodo-6-methoxy-benzamide’s behavior in different solvent environments.

Interesting facts

Interesting Facts about N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-3-iodo-6-methoxy-benzamide

The compound N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-3-iodo-6-methoxy-benzamide belongs to a unique class of chemical entities that bridge the gap between organic chemistry and medicinal applications. Here are some intriguing aspects of this compound:

  • Structural Complexity: This compound features an intricate pyrrolidine ring fused with a variety of functional groups. The presence of iodo and methoxy groups enhances its reactivity and potential biological activity.
  • Biological Relevance: Compounds containing benzamide moieties are often studied for their pharmacological properties. This particular compound might exhibit interesting interactions with biological targets, potentially influencing neurotransmitter systems.
  • Potential Applications: Due to its structural attributes, this compound may have utility in drug design, particularly in the field of neuroscience or as an anti-cancer agent. Researchers are keen to explore the biological pathways it may influence.
  • Synthetic Pathways: The synthesis of such compound can involve various organic transformations, making it a fascinating subject for those interested in synthetic organic chemistry. Understanding its formation can lead to more efficient approaches in creating similar compounds.
  • Research Opportunities: Given the constant evolution of medicinal chemistry, this compound presents various avenues for exploration—ranging from pharmacodynamics to toxicological assessments. Each investigation can yield vital insights into the compound's potential.

In conclusion, N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-3-iodo-6-methoxy-benzamide is not just an ordinary compound; it opens doors to exciting research opportunities in the realm of drug discovery and development. The ongoing study of such compounds is essential to unlock their full potential in therapeutic applications.

Synonyms
IBZM
IOLOPRIDE
CHEMBL8475
N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-3-iodo-6-methoxybenzamide
N-((1-Ethylpyrrolidin-2-yl)methyl)-2-hydroxy-3-iodo-6-methoxybenzamide
Benzamide,N-[[(2S)-1-ethyl-2-pyrrolidinyl]methyl]-2-hydroxy-3-iodo-6-methoxy-
SCHEMBL830082
N-(1-Ethyl-pyrrolidin-2-ylmethyl)-2-hydroxy-3-iodo-6-methoxy-benzamide
DTXSID60869574
BDBM50020704
130383-75-4
DB-221245
DB-255525
N-[(1-ethyl-2-pyrrolidinyl)methyl]-2-hydroxy-3-iodo-6-methoxy-benzamide