CAS 83732-75-6
:1-Methyl-1H-pyrrole-2-ethanamine
Description:
1-Methyl-1H-pyrrole-2-ethanamine, with the CAS number 83732-75-6, is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. This compound features a methyl group at the 1-position and an ethylamine side chain at the 2-position of the pyrrole ring. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the amine functional group imparts basic properties, allowing it to participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. Its structure suggests potential applications in pharmaceuticals, agrochemicals, and as a building block in organic synthesis. The compound may exhibit biological activity, making it of interest in medicinal chemistry. However, specific safety and handling guidelines should be followed, as with all chemical substances, due to potential toxicity or reactivity.
Formula:C7H12N2
InChI:InChI=1S/C7H12N2/c1-9-6-2-3-7(9)4-5-8/h2-3,6H,4-5,8H2,1H3
InChI key:InChIKey=ITFDYXKCBZEBDG-UHFFFAOYSA-N
SMILES:C(CN)C=1N(C)C=CC1
Synonyms:- 1-Methyl-1H-pyrrole-2-ethanamine
- 1-Methyl-2-(2-aminoethyl)pyrrole
- 1H-Pyrrole-2-ethanamine, 1-methyl-
- 2-(1-Methyl-1H-pyrrol-2-yl)ethan-1-amine
- 2-(1-Methylpyrrol-2-yl)ethanamine
- 2-(1-Methylpyrrol-2-yl)ethylamine
- 2-(1-methyl-1H-pyrrol-2-yl)ethanamine
- 2-(2-Aminoethyl)-1-methyl-1H-pyrrole
- 2-(2-Aminoethyl)-1-methylpyrrole
- 2-(2-Aminoethyl)-N-methylpyrrole
- N-methyl-2-(1H-pyrrol-2-yl)ethanamine
- See more synonyms
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Found 2 products.
2-(1-Methyl-1H-pyrrol-2-yl)ethanamine
CAS:<p>2-(1-Methyl-1H-pyrrol-2-yl)ethanamine</p>Purity:95%Molecular weight:124.18g/mol2-(1-Methyl-1H-pyrrol-2-yl)ethanamine
CAS:<p>2-(1-Methyl-1H-pyrrol-2-yl)ethanamine (MPEA) is a tetracoordinated cationic aminopyridine with a dimeric structure. It reacts with x-rays, showing an X-ray diffraction pattern. The crystallographic data for MPEA can be found in the PDB database under accession code 3AB6. MPEA is also synthesized from 1,4-dimethylpyrrole and ethylamine in a two step procedure with high yields. The reactivity of MPEA has been studied by reacting it with aminopyridines or amino groups and observing the products formed as well as the equilibrium conditions.</p>Formula:C7H12N2Purity:Min. 95%Molecular weight:124.19 g/mol

