Interesting facts
Interesting Facts about 2-(1-methylimidazol-4-yl)ethanamine
2-(1-methylimidazol-4-yl)ethanamine is a fascinating compound with unique properties and potential applications. Here are some engaging facts about it:
- Structural Significance: This compound features an imidazole ring, known for its role in various biological systems and as a crucial component in the structure of amino acids such as histidine.
- Biosynthetic Pathways: Compounds like 2-(1-methylimidazol-4-yl)ethanamine are often studied for their involvement in biological processes. They can act as precursors in the biosynthesis of important biomolecules.
- Pharmacological Potential: The presence of the imidazole moiety suggests that this compound may exhibit interesting pharmacological activities. Imidazole derivatives have been known to function as enzyme inhibitors and serve as ligands in medicinal chemistry.
- Research Applications: Scientists are keenly interested in this compound due to its potential use in drug development. It may serve as a model for designing new therapeutics in various fields including oncology and neurobiology.
- Reactivity: The functional groups present in the molecule allow for various chemical reactions, making it versatile in synthetic chemistry. This opens the door to the development of novel compounds for research.
- Environmental Chemistry: The stable nature of such compounds makes them relevant in environmental studies, where understanding their interactions and transformations in ecosystems is vital.
In summary, 2-(1-methylimidazol-4-yl)ethanamine is not only a molecule of academic interest but also a compound with promising applications in medicinal chemistry and biology, highlighting the interconnectedness of chemical structure and biological function.
Synonyms
1-Methylhistamine
501-75-7
Tele-methylhistamine
2-(1-methyl-1H-imidazol-4-yl)ethan-1-amine
N-Telle-methylhistamine
N1-Methylhistamine
2-(1-methyl-1H-imidazol-4-yl)ethanamine
1-Methyl-1H-imidazole-4-ethanamine
2-(1-methylimidazol-4-yl)ethanamine
1H-Imidazole-4-ethanamine, 1-methyl-
N-tele-Methylhistamine
N(sup 1)-Methylhistamine
Ntau-Methylhistamine
NSC 66736
1-Methyl-4-histamine
Imidazole, 4-(2-aminoethyl)-1-methyl-
KCB81T4EOF
1-Methyl-4-(beta-aminoethyl)imidazole
BRN 0110757
CHEBI:29009
2-(1-Methyl-1H-imidazol-4-yl)ethylamine
N(tele)-methylhistamine
1-Methyl-4-(2-aminoethyl)imidazole
NSC-66736
1H-IMIDAZOLE, 4-(1-AMINOETHYL)-1-METHYL-
DTXSID30198207
5-25-09-00527 (Beilstein Handbook Reference)
1-Methyl-4-(.beta.-aminoethyl)imidazole
1,4-methylhistamine
N-tele methylhistamine
N-[3H]methylhistamine
1-methyl-4-(b-aminoethyl)imidazole
4-(1-aminoethyl)-1-methyl-1H-imidazole
UNII-KCB81T4EOF
NT-methylhistamine
4-(2-Aminoethyl)-1-methylimidazole
MFCD01941538
N(1)-methylhistamine
Histamine, 1-methyl-
N.tau.-Methylhistamine
N( 1)-Methylhistamine
Lopac-M-4910
CHEMBL507
Lopac0_000757
SCHEMBL196356
GTPL1241
GTPL1242
SCHEMBL3826532
DTXCID20120698
NSC66736
BDBM50198912
PDSP1_000511
PDSP2_000509
2-(1-Methylimidazole-4-yl)ethanamine
4-(2-aminoethyl)-1-methyl-Imidazole
AKOS006350836
CCG-204842
HY-W062542
SB15504
SDCCGSBI-0050735.P002
NCGC00015677-01
NCGC00015677-02
NCGC00015677-03
NCGC00015677-04
NCGC00162240-01
AS-50436
H137
DB-354644
CS-0054396
NS00121316
[2-(1-methyl-1H-imidazol-4-yl)ethyl]amine
1H-Imidazole-4-ethanamine, 1-methyl-(9CI)
2-(1-Methyl-1H-imidazol-4-yl)ethylamine #
C05127
EN300-116916
Imidazole, 4-(2-aminoethyl)-1-methyl-(8CI)
P10213
L000842
Q27078070
AF9B9F65-564B-4C50-B4AF-F195114242DE
838-453-9
Solubility of 2-(1-methylimidazol-4-yl)ethanamine
2-(1-methylimidazol-4-yl)ethanamine, with the chemical formula C5H9N3, exhibits notable solubility properties due to its structural characteristics. The presence of both nitrogen atoms in the imidazole ring and the amine group enhances its interaction with polar solvents, making it highly soluble in water.
When considering the solubility of this compound, here are a few key points:
Overall, the solubility profile of 2-(1-methylimidazol-4-yl)ethanamine underscores its utility in various chemical applications. It is particularly useful in formulations requiring a soluble nitrogen base.