2-Amino-3-hydroxypyridine
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- 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
Identification
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.