2-Amino-3-hydroxypyridine

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Identification

Molecular formula
C5H6N2O
CAS Number
16867-03-1
IUPAC Name
2-aminopyridin-3-ol
Molecular Weight
110.12g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3000g/cm3
Synonyms
2-AMINO-3-HYDROXYPYRIDINE
Interesting facts

Interesting Facts about 2-Aminopyridin-3-ol

2-Aminopyridin-3-ol is a fascinating compound with diverse applications, reflecting its significance in various scientific fields. Here are some engaging insights:

Key Characteristics

  • Structural Affinity: This compound belongs to the class of aminopyridines, which are known for their potential in medicinal chemistry and material science.
  • Functional Versatility: The presence of both an amino group and a hydroxyl group allows for interesting reactivity and the ability to form hydrogen bonds, making it a valuable intermediate in organic synthesis.
  • Biological Importance: Compounds related to 2-aminopyridin-3-ol have been studied for their role in the development of pharmaceuticals, particularly in drugs targeting central nervous system disorders.

Applications and Uses

2-Aminopyridin-3-ol finds utility in several important areas:

  • Pharmaceuticals: As a building block for synthesizing bioactive molecules, it plays a vital role in drug discovery.
  • Agriculture: Research indicates potential use in agrochemicals due to its ability to interact with specific enzymes.
  • Material Science: It may serve as a precursor for novel materials with unique properties.

Chemical Behavior

The compound demonstrates intriguing chemical behavior, such as:

  • Protonation: The amino group can be protonated under acidic conditions, expanding its reactivity.
  • Reactivity: With electrophiles, its nucleophilic site on the amino group makes it a target for substitution reactions.

Overall, 2-aminopyridin-3-ol exemplifies the intricate connection between structure and function, showcasing why scientists and researchers are drawn to its study.

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