5-bromo-3-(piperidin-1-yl)pyrazin-2-amine
$250.00
CAS No.: 90674-84-3
Catalog No.: 196304
Purity: 95%
MF: C9H13BrN4
MW: 257.135
Storage: 2-8 degree Celsius
SMILES: BrC=1N=C(C(=NC1)N)N1CCCCC1
Catalog No.: 196304
Purity: 95%
MF: C9H13BrN4
MW: 257.135
Storage: 2-8 degree Celsius
SMILES: BrC=1N=C(C(=NC1)N)N1CCCCC1
5-bromo-3-(piperidin-1-yl)pyrazin-2-amine; CAS No.: 90674-84-3; 5-bromo-3-(piperidin-1-yl)pyrazin-2-amine. PROPERTIES: This compound presents a 5-bromo-3-(piperidin-1-yl)pyrazin-2-amine structure, combining a bromine atom, a piperidine group, and a pyrazine framework. It typically appears as a white to off-white crystalline solid with a molecular weight of approximately 253.0 g/mol (C8H10BrN5). The melting point ranges between 180-185 C, and it exhibits moderate solubility in common organic solvents like DMSO and DMF while being sparingly soluble in water. Proper storage requires a tightly sealed container in a cool, dry place. Safety considerations include wearing appropriate PPE. It is classified as a skin and eye irritant (GHS07) with the hazard statement H315-H319. APPLICATIONS: 5-Bromo-3-(piperidin-1-yl)pyrazin-2-amine serves as a specialized intermediate in pharmaceutical research. Its 5-bromo-3-(piperidin-1-yl)pyrazin-2-amine structure enables diverse reactivity patterns, including palladium-catalyzed cross-coupling reactions at the bromine position and nucleophilic substitution at the pyrazine ring. In medicinal chemistry, it is used to develop bioactive molecules targeting kinases, proteases, and G protein-coupled receptors. The bromine atom provides a handle for introducing aryl, vinyl, or heterocyclic substituents. This compound also functions as a building block in the synthesis of fluorescent dyes and bioconjugation reagents. Academic studies utilize it as a model system in Medicinal Chemistry journals, focusing on optimizing the 5-bromo-3-(piperidin-1-yl)pyrazin-2-amine scaffold for improved biological activity and target engagement.
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