Interesting facts
Interesting Facts about Pyridine-3,4-Diamine
Pyridine-3,4-diamine, also known as 3,4-diaminopyridine, is a fascinating compound with a rich involvement in both chemistry and biotechnology. Here are some engaging insights about this unique molecule:
- Structural Significance: Pyridine-3,4-diamine features a pyridine ring, a six-membered aromatic heterocycle with nitrogen atoms. This ring structure plays a crucial role in its chemical reactivity and interactions.
- Biological Relevance: This compound is notable for its role in medicinal chemistry. With potential applications in treating neurological disorders such as Lambert-Eaton Myasthenic Syndrome (LEMS), it enhances neurotransmitter release, making it a subject of ongoing research.
- Synthesis Variability: Pyridine-3,4-diamine can be synthesized through various methods, including the reduction of the corresponding pyridine-3,4-dicarboxylic acid and other multi-step organic reactions. This flexibility in synthesis makes it an interesting target for chemists.
- Pharmacological Potential: Beyond its neurological applications, there is promising research that explores its effectiveness against certain types of cancer. This adaptability underscores the importance of studying small organic molecules in drug development.
As chemists and researchers delve deeper into the properties and applications of pyridine-3,4-diamine, the compound continues to inspire innovations in both materials science and medicine. Truly, the world of chemical compounds like pyridine-3,4-diamine offers endless opportunities for discovery!
Synonyms
3,4-DIAMINOPYRIDINE
pyridine-3,4-diamine
54-96-6
Amifampridine
3,4-Pyridinediamine
3,4-DAP
4,5-Diaminopyridine
Diamino-3,4 pyridine
Pyridine, 3,4-diamino-
amifampridin
SC10
Dynamine
Ruzurgi
3,4 Diaminopyridine
amifampridina
UNII-RU4S6E2G0J
EINECS 200-220-9
RU4S6E2G0J
NSC 521760
NSC-521760
BRN 0110232
DTXSID6046715
3-amino-4-pyridinylamine
MFCD00006401
54-96-6 (free base)
CHEMBL354077
DTXCID4026715
5-22-11-00266 (Beilstein Handbook Reference)
NSC521760
NCGC00167560-01
AMIFAMPRIDINE (MART.)
AMIFAMPRIDINE [MART.]
CAS-54-96-6
SMR000752913
Amifampridine [INN]
amifampridinum
Amifampridine [USAN:INN:BAN]
Ruzurgi (TN)
Pyridine,4-diamino-
3,4-diamino pyridine
3,4-diamino-pyridine
3,4-Diammoniopyridinium
pyridine, 4,5-diamino-
AMIFAMPRIDINE [MI]
WLN: T6NJ CZ DZ
Amifampridine (USAN/INN)
4-DAP
AMIFAMPRIDINE [USAN]
SCHEMBL21273
MLS001304911
MLS001333181
MLS001333182
AMIFAMPRIDINE [WHO-DD]
GTPL8032
AMIFAMPRIDINE [EMA EPAR]
N07XX05
CHEBI:135948
HMS2233K06
AMIFAMPRIDINE [ORANGE BOOK]
ALBB-005969
BCP22343
Tox21_112555
3,4 DIAMINOPYRIDINE [VANDF]
BBL013269
BDBM50416493
CL0116
NSC790505
s4622
STK503647
AKOS000672436
Tox21_112555_1
CCG-304141
DB11640
FD07065
NSC-790505
PB48915
PS-9273
NCGC00167560-02
BP-12781
HY-14946
3,4-Diamino[3,4-?]pyridine;Amifampridine
DB-011105
A7976
D1149
NS00021207
EN300-69695
D10228
AC-907/34116043
Q411707
BRD-K80262108-001-07-0
F0001-1409
Z385438794
InChI=1/C5H7N3/c6-4-1-2-8-3-5(4)7/h1-3H,7H2,(H2,6,8
200-220-9
L89
Solubility of Pyridine-3,4-diamine (C5H7N3)
Pyridine-3,4-diamine, a derivative of pyridine featuring two amino groups, exhibits notable solubility characteristics that are influenced by its molecular structure. Here are some key points regarding its solubility:
In summary, pyridine-3,4-diamine's solubility is fundamentally shaped by its functional groups, allowing it to interact favorably with polar solvents. This property aids in its utility across various chemical and pharmaceutical applications, showcasing the importance of solubility in practical scenarios.