Interesting facts
Interesting Facts about Pyridine-2,6-diamine
Pyridine-2,6-diamine, also known as 2,6-diaminopyridine, is an intriguing organic compound that belongs to the family of pyridines, which are aromatic heterocyclic compounds. Here are some captivating insights about this compound:
- Structure and Isomerism: Pyridine-2,6-diamine features two amino groups (-NH2) positioned at the 2 and 6 carbon atoms of the pyridine ring. This unique arrangement leads to interesting structural properties and reactivity patterns.
- Biological Significance: This compound is notable for its potential biological activities, including its roles as a signaling molecule in various biochemical pathways. Researchers study its effects on neuron function and muscle regeneration, making it a focus in medicinal chemistry.
- Applications in Material Science: Due to its functional groups, pyridine-2,6-diamine can serve as a valuable building block in the synthesis of polymers and advanced materials, imparting unique properties such as improved solubility and thermal stability.
- Chemical Reactivity: The presence of amine functional groups in this compound enables it to participate in several chemical reactions, including acylation and alkylation. This reactivity allows chemists to design and synthesize new derivatives with tailored properties.
- Analytical Techniques: Pyridine-2,6-diamine can be analyzed using various techniques such as NMR spectroscopy and mass spectrometry. These methods provide insights into its structural characteristics and purity, which are crucial for quality control in research and industry.
As a chemical scientist or student, understanding the properties and applications of pyridine-2,6-diamine can open pathways to innovative research and advancements in diverse fields such as organic synthesis, pharmacology, and materials science. Its versatility and fascinating chemistry make it a compound worth exploring further.
Synonyms
2,6-Diaminopyridine
141-86-6
pyridine-2,6-diamine
2,6-pyridinediamine
pyridine-2,6-diyldiamine
DAP (amine)
pyridine, 2,6-diamino-
CCRIS 6682
Diaminopyridine, 2,6-
UNII-K89AB8CKG6
NSC 1921
EINECS 205-507-2
K89AB8CKG6
MFCD00006329
BRN 0108513
2,6-Diamino pyridine
DTXSID0040127
AI3-18054
NSC-1921
RODOL 26PYR
118352-40-2
DIAMINOPYRIDINE [VANDF]
26-DAP
DTXCID8020127
5-22-11-00255 (Beilstein Handbook Reference)
2-Pyridinamine,1,6-dihydro-6-imino-,(E)-(9CI)
118352-39-9
26D
2-Pyridinamine,1,6-dihydro-6-imino-,(Z)-(9CI)
CAS-141-86-6
diaminopyridines
2,6Pyridinediamine
Pyridine2,6diamine
2,6-diaminopyrdine
2,6-diamino-pyridine
Pyridine2,6diyldiamine
2, 6-Diaminopyridine
Pyridine, 2,6diamino
6-amino-2-iminopyridine
WLN: T6NJ BZ FZ
SCHEMBL64599
2,6-Diaminopyridine, 98%
BIDD:GT0354
2,6DAP
CHEMBL339234
CHEBI:51598
2,6-DAP
NSC1921
BCP27453
HY-Y0198
STR00979
2,6-DIAMINOPYRIDINE [INCI]
Tox21_201654
Tox21_303403
BBL011548
MSK000225
STL146681
AKOS000119875
CS-W020019
FD00549
PS-9269
NCGC00249093-01
NCGC00257467-01
NCGC00259203-01
AC-10706
DB-013980
D1154
NS00013560
EN300-21301
D77864
AC-907/25014391
2,6-Diaminopyridine 100 microg/mL in Acetonitrile
2,6-Diaminopyridine, Vetec(TM) reagent grade, 98%
Q15725608
F8881-0498
Z104495224
Solubility of Pyridine-2,6-diamine
Pyridine-2,6-diamine, also known as 2,6-diaminopyridine, is a compound characterized by its unique solubility properties. With the chemical formula C5H7N3, it demonstrates varying degrees of solubility depending on the solvent used:
Overall, the solubility of pyridine-2,6-diamine is influenced by factors such as temperature and pH, as well as the presence of different ionic or molecular species in the solution. This is important to consider when designing experiments or industrial processes involving this compound.