Norephedrine
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- Molecular formula
- C9H13NO
- CAS Number
- 700-12-9
- IUPAC Name
- 2-(isopropylamino)-1-phenyl-ethanol
- Molecular Weight
- 151.21g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0950g/cm3
- Synonyms
- 4164-21-0
Identification
Interesting facts
Interesting Facts about 2-(Isopropylamino)-1-phenyl-ethanol
2-(Isopropylamino)-1-phenyl-ethanol, often referred to in research contexts for its intriguing properties and potential applications, is a compound that stands out in the realm of chemical science. Here are some fascinating insights:
- Biological Importance: This compound has been of interest in pharmacology due to its structural resemblance to various drugs, potentially influencing biological systems.
- Chirality: The molecule can exhibit chirality, meaning it may have two mirror-image forms (enantiomers), which can result in different biological responses. This is a crucial concept in medicinal chemistry, as often one enantiomer is therapeutically active while the other may not be.
- Synthetic Routes: Scientists have explored multiple synthetic pathways to create this compound, including the use of asymmetric synthesis, which highlights its complexity and the ingenuity of chemists at work.
- Applications in Research: 2-(Isopropylamino)-1-phenyl-ethanol serves as a valuable intermediate in the synthesis of other organic compounds, demonstrating its utility in various chemical reactions.
- Potential Side Effects: When considering its pharmacological potential, research into side effects and toxicity is essential, illustrating the balance required in drug development.
Overall, the exploration of 2-(isopropylamino)-1-phenyl-ethanol opens up discussions about the interplay between molecular structure and biological function, offering insights that could pave the way for new therapies and research methodologies.