2-(N-benzylanilino)-N'-hydroxy-acetamidine

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Identification

Molecular formula
C15H17N3O
CAS Number
. CAS number not available
IUPAC Name
2-(N-benzylanilino)-N'-hydroxy-acetamidine
Molecular Weight
238.32g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2030g/cm3
Synonyms
25394-78-9
Interesting facts

Interesting Facts about 2-(N-benzylanilino)-N'-hydroxy-acetamidine

2-(N-benzylanilino)-N'-hydroxy-acetamidine, a fascinating compound, has garnered the attention of chemists due to its unique structure and potential applications. Here are some engaging insights about this compound:

  • Structure and Functionality: The compound possesses a complex structure characterized by the presence of a hydroxylamine group, which enhances its reactivity. This structure enables the compound to participate in various chemical reactions, making it versatile in synthetic pathways.
  • Biological Relevance: Compounds similar to this one have been investigated for their biological activities, particularly as potential pharmaceuticals. They might exhibit properties such as anti-cancer and anti-inflammatory effects, which is crucial for drug discovery.
  • Research Applications: The compound is of interest in materials science and organic synthesis due to its ability to form hydrogen bonds. This quality makes it a candidate for developing new materials with desired thermal and mechanical properties.
  • Historical Context: Hydroxy-acetamidine derivatives have been part of research for many years, often used to create more complex organic compounds that could lead to breakthroughs in both medicinal and material chemistry.

“Understanding complex compounds like 2-(N-benzylanilino)-N'-hydroxy-acetamidine can lead to innovative solutions and advancements in various scientific fields.”

In summary, 2-(N-benzylanilino)-N'-hydroxy-acetamidine stands out for its intriguing chemical properties and potential applications that span across various domains within chemistry. Its ongoing study promises to reveal more about its utility and effects, fostering advancements in scientific research.

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