Interesting facts
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.
“The pursuit of understanding chemical nature is what distinguishes chemistry from mere observation.” — Anonymous
Synonyms
2,5-DIAMINOPYRIDINE
4318-76-7
PYRIDINE-2,5-DIAMINE
2,5-Pyridinediamine
Pyridine, 2,5-diamino-
H6OLZ060HI
NSC 175741
BRN 0108741
NSC-175741
DTXSID20195765
5-22-11-00252 (Beilstein Handbook Reference)
J51.294J
2,5-Pyridinediamine (9CI)
DTXCID60118256
626-246-4
MFCD00129023
2 pound not5-Diaminopyridine
UNII-H6OLZ060HI
Pyridine,5-diamino-
2,5-diamino pyridine
2,5-diamino-pyridine
WLN: T6NJ BZ EZ
SCHEMBL34048
YSZC148
2,5-Diaminopyridine, 97%
SCHEMBL24077008
GEO-04049
NSC175741
AKOS007930448
AC-5938
CS-W011281
SB75612
AS-13208
DA1
FD153008
SY030543
DB-031536
EN300-156258
AC-907/25014078
Q27279708
Z385438796
Solubility of Pyridine-2,5-diamine
Pyridine-2,5-diamine, also known by its systematic name 2,5-diaminopyridine, is a heterocyclic organic compound with distinctive solubility characteristics.
Water Solubility
This compound exhibits decent solubility in water, which can be attributed to the presence of amino groups that can form hydrogen bonds with water molecules. Here are some key points regarding its solubility:
Solvent Affinity
Beyond water, pyridine-2,5-diamine is known to dissolve well in various organic solvents, making it versatile for a range of applications. Its affinity for solvents includes:
In conclusion, the solubility of pyridine-2,5-diamine is influenced by multiple factors including temperature, pH, and the nature of solvents. Its ability to interact with water and other solvents through hydrogen bonding and dipole interactions makes it a noteworthy compound in chemical applications.