2,5-Diaminopyridine
- Molecular formula
- C5H7N3
- CAS Number
- 141-86-6
- IUPAC Name
- pyridine-2,5-diamine
- Molecular Weight
- 109.13g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2110g/cm3
- Synonyms
- 2, 5-DIAMINOPYRIDINE
Identification
Interesting Facts about Pyridine-2,5-Diamine
Pyridine-2,5-diamine, often recognized for its unique structure and properties, has made significant contributions to various fields of chemistry, particularly in pharmaceuticals and agrochemicals. Here are some intriguing aspects of this compound:
- Structural Characteristics: Pyridine-2,5-diamine features a pyridine ring that is complemented by amino groups at the 2nd and 5th positions. This unique substitution pattern influences its reactivity and interactions.
- Biological Significance: This compound is known for its potential role in drug synthesis, where it serves as a key building block in the production of several bioactive molecules.
- Catalytic Applications: Pyridine derivatives, including pyridine-2,5-diamine, are utilized in coordination chemistry as ligands in catalysts, aiding in the transformation of substrates in various reactions.
- Research Interest: Organic chemists are particularly interested in this compound due to its ability to act as a nucleophile, allowing it to participate in a range of chemical reactions such as nucleophilic substitutions and coupling reactions.
- Environmental Implications: Its derivatives are also studied for use in agriculture as herbicides and fungicides, demonstrating efficacy in pest management systems.
In summary, pyridine-2,5-diamine is not just an ordinary compound; its multifaceted roles in research, pharmaceuticals, and agriculture underscore its importance in both scientific and practical applications. As scientists continue to explore its potential, it emphasizes the critical balance between innovation and environmental stewardship.
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