Interesting facts
Interesting Facts about Pyridin-2-amine
Pyridin-2-amine, often referred to as 2-aminopyridine, is a fascinating aromatic amine that showcases some intriguing properties and applications in various fields. Here are some key points that highlight the importance and versatility of this compound:
- Structure and Properties: Pyridin-2-amine contains a pyridine ring substituted at the 2-position with an amino group. This positioning is crucial as it affects the compound's reactivity and interactions.
- Chemical Reactivity: The amino group (-NH2) confers basic properties to the molecule, allowing it to participate in various chemical reactions, including nucleophilic substitutions and condensation reactions.
- Biological Significance: Pyridin-2-amine derivatives have been the subject of extensive research due to their potential medicinal properties, including anti-inflammatory and neuroprotective effects. Researchers are exploring their potential as drug candidates in various therapeutic areas.
- Synthetic Routes: There are several methods for synthesizing pyridin-2-amine, including the reduction of 2-cyanopyridine or direct amination of pyridine, showcasing the compound's accessibility for further chemical modification.
- Applications in Material Science: Beyond organic chemistry and medicinal applications, pyridin-2-amine and its derivatives are being investigated for their use in creating advanced materials, such as polymers and functional coatings.
In conclusion, pyridin-2-amine stands as a compelling example of how simple organic compounds can lead to significant advancements in both scientific research and practical applications. As scientists continue to explore its potential, we may uncover even more exciting uses for this versatile compound.
Synonyms
2-AMINOPYRIDINE
504-29-0
pyridin-2-amine
2-Pyridinamine
2-Pyridylamine
Pyridinamine
Aminopyridine
o-Aminopyridine
2-aminopyridin
2-Aminopryidine
Pyridine, 2-amino-
Amino-2 pyridine
1,2-Dihydro-2-iminopyridine
2-Pyridinylnitrene
26445-05-6
Pyridin-2-ylamine
.alpha.-Aminopyridine
NSC 431
2-pyridinylamine
.beta.-Pyridylamine
pyridin-2-yl-amine
.alpha.-Pyridinamine
.alpha.-Pyridylamine
MFCD00006312
WSX981HEWU
CHEMBL21619
DTXSID0024505
NSC-431
2-amino pyridine
alpha-Pyridinamine
alpha-Pyridylamine
alpha-Aminopyridine
24843-39-8
Pyridin-2-amine (2-Pyridylamine)
Pyridine, amino-
CCRIS 4747
HSDB 2068
EINECS 207-988-4
UNII-WSX981HEWU
aminopyridin
iminopyridine
pyridineamine
pyridinylamine
Aminopyridines
amino pyridine
amino-pyridine
Pyridyl amine
pyridyl nitrogen
AI3-15287
|A-Pyridylamine
2-pyridyl amine
2-amino-pyridine
2-aminopyr-idine
pyridine-2-amine
pyridine-2-ylamine
aminopyridine, 2-
2-Aminopyridine, 99%
EC 207-988-4
2-Aminopyridine, >=99%
BIDD:GT0578
DTXCID404505
NSC431
2-AMINOPYRIDINE [HSDB]
JGQBNAFULRKENS-UHFFFAOYSA-N
.ALPHA.-AMINOPYRIDINE [MI]
BCP22964
STR00201
Tox21_200880
BBL011573
BDBM50013712
STK286012
AKOS000119615
CS-W020569
FA07684
PB47078
2-AP, 2-Pyridinamine, 2-Pyridylamine
o-Aminopyridine [UN2671] [Poison]
NCGC00248863-01
NCGC00258434-01
BP-13063
CAS-504-29-0
PD180348
PIROXICAM IMPURITY A [EP IMPURITY]
TENOXICAM IMPURITY A [EP IMPURITY]
2-Aminopyridine, purum, >=98.0% (NT)
DB-020545
A0411
NS00010856
EN300-19030
F90389
P17100
AC-907/25014346
2-Aminopyridine, PESTANAL(R), analytical standard
MEPYRAMINE MALEATE IMPURITY C [EP IMPURITY]
Q2393470
F1995-0206
PIROXICAM RELATED COMPOUND A, REFERENCE STANDARD
Z104472278
InChI=1/C5H6N2/c6-5-3-1-2-4-7-5/h1-4H,(H2,6,7
Mepyramine impurity C, European Pharmacopoeia (EP) Reference Standard
Solubility of Pyridin-2-amine
Pyridin-2-amine, also known as 2-aminopyridine, is a heterocyclic organic compound that exhibits interesting solubility properties. It is a polar compound due to the presence of the amino group (-NH2) attached to the pyridine ring, which enhances its interaction with solvents. Here are some key points to consider regarding its solubility:
In summary, pyridin-2-amine is a soluble compound in water and a variety of organic solvents, which contributes to its utility in various chemical applications. Its ability to interact with different solvents is a testament to its chemical structure and properties.