2-(Aminoethyl)-1-N-Boc-pyrrolidine is a chemical compound characterized by its pyrrolidine ring, which is a five-membered nitrogen-containing heterocycle. The "N-Boc" (tert-butoxycarbonyl) group is a common protecting group for amines, providing stability and preventing unwanted reactions during synthetic processes. This compound features an aminoethyl side chain, which contributes to its reactivity and potential applications in organic synthesis, particularly in the development of pharmaceuticals and biologically active molecules. The presence of the amino group allows for further functionalization, while the Boc group can be removed under acidic conditions to yield the free amine. Its molecular structure and functional groups make it a versatile intermediate in the synthesis of various compounds, including peptides and other nitrogen-containing heterocycles. Additionally, the compound's solubility and stability in different solvents can influence its reactivity and application in laboratory settings. Overall, 2-(Aminoethyl)-1-N-Boc-pyrrolidine is an important building block in medicinal chemistry and organic synthesis.

2-(Aminoethyl)-1-N-Boc-pyrrolidine

370069-29-7: 2-(2-Aminoethyl)pyrrolidine-1-carboxylic acid tert-butyl ester, Tert-Butyl 2-(2-Aminoethyl)Pyrrolidine-1-Carboxylate

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CAS 370069-29-7: 2-(Aminoethyl)-1-N-Boc-pyrrolidine

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