Interesting Facts about 4-[(1S)-1-hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol
This compound, commonly known as an important precursor in the synthesis of pharmaceuticals, boasts a variety of intriguing characteristics that make it a subject of scientific interest. Here are some noteworthy points:
- Pharmacological Relevance: The compound is often studied for its role as a beta-blocker, which can influence heart rate and blood pressure. This makes it potentially crucial in the treatment of cardiovascular disorders.
- Synthetic Intermediary: Due to its structural attributes, this compound serves as an essential intermediate in synthesizing other complex organic molecules.
- Chirality: It contains a chiral center, which means it exists in different enantiomeric forms. This has implications for its biological activity, as different enantiomers can exhibit varying effects in biological systems.
- Hydroxyl Groups: The presence of multiple hydroxyl groups in its structure contributes to its chemical reactivity and solubility in polar solvents, making it versatile for numerous chemical applications.
As a scientist or a chemistry student, understanding this compound not only broadens your knowledge of organic chemistry but also emphasizes the intricate relationships between molecular structure and biological function. "One molecule can change everything," is a sentiment echoed in the realm of drug discovery, illustrating the potential that compounds like this hold in advancing medical science. Explore the possibilities of this compound, as it underpins many innovative research avenues in pharmacology and organic synthesis.
Solubility of 4-[(1S)-1-hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol (C9H13NO3)
The solubility of 4-[(1S)-1-hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol can be described as moderate to good in various solvents. This compound, known for its functional groups and hydrophilic nature, shows a distinct solubility pattern:
The ability of 4-[(1S)-1-hydroxy-2-(isopropylamino)ethyl]benzene-1,2-diol to dissolve in different solvents can be attributed to the balance between its hydrophilic and hydrophobic regions. According to solubility theory, "like dissolves like," meaning that solvents with comparable polarities are likely to dissolve this compound effectively.
Overall, the solubility of this compound is fundamentally related to its molecular structure and the presence of functional groups capable of hydrogen bonding and dipole interactions. Understanding these solubility characteristics is crucial for practical applications in pharmaceuticals and chemical synthesis.