Norephedrine

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Identification

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
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.

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