Interesting facts
Interesting Facts about 2-Pyridylmethanamine
2-Pyridylmethanamine, also known as 2-(pyridin-2-yl)ethan-1-amine, is an intriguing organic compound within the realm of medicinal and synthetic chemistry. Here are some notable aspects:
- Biological Roles: This compound has been studied for its potential biological activities, including antibacterial and antifungal properties, making it a candidate for pharmaceutical applications.
- Functional Group Presence: Featuring both an amine and a pyridine ring, 2-pyridylmethanamine is an example of a compound with diverse functional groups, which can lead to varied reactivities and interactions.
- Synthesis: It can be synthesized through the alkylation of pyridine derivatives, which showcases the versatility of synthetic methodologies in organic chemistry.
- Research Applications: Chemical researchers often use this compound in studies related to enzyme inhibition, providing insights into the development of new therapeutic agents.
- Multi-faceted Utility: Beyond medicinal chemistry, 2-pyridylmethanamine can be utilized in the synthesis of agrochemicals and as a ligand in coordination chemistry, illustrating its wide-ranging applicability.
Overall, the study of 2-pyridylmethanamine illustrates the intersection of organic synthesis and medicinal application, underlining the importance of compounds that can lead to significant advancements in various scientific fields. It serves as a reminder of the vast possibilities that organic chemistry offers!
Synonyms
3731-51-9
2-(Aminomethyl)pyridine
2-Pyridinemethanamine
2-Picolinamine
2-Pyridinemethylamine
2-Pyridylmethylamine
(2-Pyridylmethyl)amine
beta-Picolylamine
NSC 59705
PYRIDINE, 2-AMINOMETHYL-
EINECS 223-090-5
BRN 0108054
2-(aminomethyl) pyridine
DTXSID5063152
5-22-09-00232 (Beilstein Handbook Reference)
2picolylamine
betaPicolylamine
2Picolinamine
2-picolamine
2pyridylmethylamine
2aminomethylpyridine
2Pyridinemethanamine
2Pyridinemethylamine
(2Pyridylmethyl)amine
Pyridine, 2aminomethyl
DTXCID4039314
223-090-5
inchi=1/c6h8n2/c7-5-6-3-1-2-4-8-6/h1-4h,5,7h
2-Picolylamine
pyridin-2-ylmethanamine
2-Aminomethylpyridine
Pyridine, 2-(aminomethyl)-
1-(pyridin-2-yl)methanamine
2-AMINOMETHYL-PYRIDINE
2-pyridinylmethylamine
MFCD00006360
(pyridin-2-yl)methanamine
C-Pyridin-2-yl-methylamine
2-Pyridinylmethanamine
(pyridin-2-ylmethyl)amine
1-pyridin-2-ylmethanamine
XK7252M2PA
CHEBI:81387
NSC-59705
Pyridinemethanamine
pyridylmethylamine
Pyridin-2-Yl-Methanamine
picolinamine
picolylamine
o-Picolylamine
2-picolyl amine
Aminomethylpyridine
aminomethyl pyridine
2-pyridylmethanamine
.beta.-Picolylamine
2-aminomethylpryidine
.alpha.-Picolylamine
2-aminomethyl pyrdine
2-pyridyl-methylamine
2(aminomethyl)pyridine
2-amino methylpyridine
2-aminomethyl pyridine
pyridine-2-methylamine
(2-pyridyl)methanamine
pyridin-2-ylmethylamine
2-(amino)methylpyridine
2-(aminomethyl)pryidine
2-amino methyl pyridine
pyridine-2-ylmethanamine
pyridine-2-ylmethylamine
2-Picolylamine, 99%
(2-pyridinylmethyl)amine
pyridin-2-ylmethyl amine
2-(amino methyl)pyridine
2-(aminomethyl)-pyridine
1-pyridin-2-ylmethaneamine
2-(amino methyl) pyridine
alpha-(Aminomethyl)pyridine
(pyridin-2-ylmethyl)-amine
WLN: T6NJ B1Z
C-pyridine-2-yl-methylamine
UNII-XK7252M2PA
SCHEMBL40328
CHEMBL32189
SCHEMBL2086329
(PYRIDIN-2-YL)METHYLAMINE
NSC59705
STK802385
AKOS000118825
AB00731
BCP9000115
CS-W007488
FP34672
PS-9292
BP-12086
DB-015973
A1161
NS00030176
EN300-19584
2-(Aminomethyl)pyridine 2-Pyridinemethaneamine
C17926
F11236
Q27155325
F2190-0394
Z104474352
2-Picolylamine, for HPLC derivatization, >=98.0% (GC)
Solubility of 2-pyridylmethanamine
2-pyridylmethanamine, also referred to as 2-(pyridin-2-yl)ethanamine, demonstrates notable solubility characteristics that can be categorized based on its chemical structure and functional groups.
Key Points on Solubility:
Moreover, the solubility can be affected by several factors, including:
In summary, 2-pyridylmethanamine exhibits a distinctive solubility profile, highlighting its capabilities to dissolve in both polar and non-polar environments due to its unique functional groups. This makes it versatile for a range of chemical applications.