N-(9H-fluoren-3-yl)-N-hydroxy-acetamide

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Identification

Molecular formula
C15H13NO2
CAS Number
153640-55-4
IUPAC Name
N-(9H-fluoren-3-yl)-N-hydroxy-acetamide
Molecular Weight
255.28g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2000g/cm3
Synonyms
N-Hydroxy-3-fluorenylacetamide
Interesting facts

Interesting Facts about N-(9H-fluoren-3-yl)-N-hydroxy-acetamide

N-(9H-fluoren-3-yl)-N-hydroxy-acetamide is a fascinating chemical compound that blends the characteristics of a hydroxyamide with the structural complexity of a fluorenyl moiety. This unique combination gives rise to several intriguing properties and potential applications. Here are some noteworthy points:

  • Versatile Building Block: The fluorenyl group in this compound serves as a versatile building block for the synthesis of various derivatives, making it a valuable intermediate in organic chemistry.
  • Biological Relevance: Hydroxyamides like this one often feature in biological systems, leading to interesting studies in drug design and medicinal chemistry, where they may act as enzyme inhibitors.
  • Fluorescent Properties: The fluorenyl part of the molecule is known for its fluorescence, which opens possibilities for applications in fluorescence microscopy and tracking biological processes.
  • Research Applications: This compound is used in various research fields, including material science, due to its stability and unique chemical behavior, which can be harnessed for creating novel materials.
  • Structural Studies: By studying the interactions and conformations of N-(9H-fluoren-3-yl)-N-hydroxy-acetamide, researchers can gain insights into structure-activity relationships important for designing new compounds with desired properties.

As a chemist or a student, one may ponder the potential innovations that such compounds might bring to the fields of chemistry and biology. The ongoing study of N-(9H-fluoren-3-yl)-N-hydroxy-acetamide emphasizes the profound impact that organic compounds can have on advancing science and technology.

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