Benzoxazocinol

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Identification

Molecular formula
C16H17NO2
CAS Number
1224690-84-7
IUPAC Name
6-(2-phenylethyl)-3,4-dihydro-2H-1,5-benzoxazocin-3-ol
Molecular Weight
251.32g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3210g/cm3
Synonyms
BRN 4915881
Interesting facts

6-(2-phenylethyl)-3,4-dihydro-2H-1,5-benzoxazocin-3-ol

This intriguing compound, known as a benzoxazocin, brings together both aromatic and heterocyclic chemistry, showcasing the complexity and beauty of organic molecules. The structural framework of this compound includes:

  • A benzoxazocin system, which is a bicyclic structure that contains both a benzene ring and a nitrogen-oxygen heterocycle.
  • A 2-phenylethyl substituent that introduces an aromatic hydrocarbon into the molecular architecture, greatly influencing the compound's properties.
  • An alcohol functional group that enhances its reactivity in various chemical reactions.

What makes 6-(2-phenylethyl)-3,4-dihydro-2H-1,5-benzoxazocin-3-ol particularly interesting are its potential applications and biological activities. For instance:

  • Compounds containing benzoxazocin frameworks have been investigated for their roles in medicinal chemistry, particularly in the development of new pharmaceuticals.
  • The presence of the phenylethyl group may increase its biological activity, as this moiety is often associated with various biological effects.
  • Research suggests that derivatives of this class may possess antioxidant and anti-inflammatory properties, making them candidates for therapeutic exploration.

Furthermore, the synthesis of compounds like 6-(2-phenylethyl)-3,4-dihydro-2H-1,5-benzoxazocin-3-ol serves as an excellent example of the principles of organic synthesis in action. The combination of traditional reduction reactions to form alcohols alongside aromatic substitutions exemplifies the creativity and finesse required in contemporary chemistry.

Overall, this compound invites further study and exploration, highlighting the intricate dance between structure and function in the realm of chemical research.

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