Interesting facts
Interesting Facts about 3,5-Dichloro-N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-6-methoxy-benzamide
This chemical compound is particularly fascinating due to its unique structural features and potential applications in medicinal chemistry. Here are some noteworthy points to consider:
- Dual Action: The compound features both a dichloro (Cl) and methoxy (OCH3) functional group, which can enhance its biological activity and specificity in target interactions, making it interesting for pharmaceutical research.
- Biological Relevance: Compounds like these are often studied for their roles in drug development, especially in the field of neuropharmacology. Its pyrrolidine ring can suggest potential effects on the central nervous system.
- Structure-Activity Relationship (SAR): Understanding how modifications to this compound affect biological activity is a key area of study. The combination of different functional groups can significantly alter the interaction with biological targets.
- Research Applications: The unique chemical structure of 3,5-dichloro-N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-6-methoxy-benzamide makes it a candidate for research in developing novel therapeutics for various conditions.
- Synthesis Complexity: The synthesis of such a complex molecule often requires multi-step organic synthesis techniques, showcasing the ingenuity and skill in modern chemistry laboratories.
As a chemistry student or scientist, the study of this compound not only deepens your understanding of complex organic structures but also opens avenues in drug development, making this compound a valuable subject for further research and exploration.
In the words of chemist Robert H. Grubbs, "Chemistry is the science of transformation," and compounds like this exemplify that transformative power in a biological context.
Synonyms
3,5-dichloro-N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-6-methoxybenzamide
SCHEMBL7472330
DTXSID50861067
3,5-Dichloro-N-(1-ethyl-pyrrolidin-2-ylmethyl)-2-hydroxy-6-methoxy-benzamide(Raclopride)
WAOQONBSWFLFPE-UHFFFAOYSA-N
HMS3370D08
HMS3393C03
BDBM50010637
AKOS040759207
LS-14414
L000503
(-)-N-Ethyl-2-(3,5-dichloro-6-hydroxy-2-methoxybenzamidomethyl)pyrrolidine
3,5-dichloro-N-(1-ethylpyrrolidin-2-ylmethyl)-2 hydroxy-6-methoxybenzamide
(S)-3,5-Dichloro-N-(1-ethyl-pyrrolidin-2-ylmethyl)-2-hydroxy-6-methoxy-benzamide(raclopride)
Solubility of 3,5-Dichloro-N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-6-methoxy-benzamide
The solubility of 3,5-dichloro-N-[(1-ethylpyrrolidin-2-yl)methyl]-2-hydroxy-6-methoxy-benzamide (C15H19Cl2N2O3) is influenced by various factors, particularly its molecular structure and the presence of polar and non-polar functional groups. This compound exhibits characteristics that suggest it may have limited solubility in water, primarily due to:
In general, this compound is expected to demonstrate:
Researchers might consider utilizing co-solvents or pH adjustments to enhance the solubility, as the interplay between ionic and non-ionic character plays a crucial role in the dissolution process. As a final note, understanding the solubility behavior of this compound is vital for applications in pharmaceuticals and material sciences, as it impacts bioavailability and compound stability.