1-Boc-3-(aminomethyl)pyrrolidine is a chemical compound characterized by its pyrrolidine ring, which is a five-membered saturated nitrogen-containing heterocycle. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group for amines, indicating that the compound has a protected amine functionality. The presence of the aminomethyl group at the 3-position of the pyrrolidine ring suggests that it can participate in various chemical reactions, making it useful in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. This compound is typically a white to off-white solid and is soluble in organic solvents. Its molecular structure allows for potential interactions in biological systems, which may be of interest in medicinal chemistry. Additionally, the compound's stability and reactivity can be influenced by the Boc group, which can be removed under acidic conditions to yield the free amine. Overall, 1-Boc-3-(aminomethyl)pyrrolidine serves as a versatile intermediate in synthetic chemistry.

1-Boc-3-(aminomethyl)pyrrolidine

270912-72-6: (R)-1-Boc-3-(aminomethyl)pyrrolidine, Tert-Butyl 3-(Aminomethyl)Pyrrolidine-1-Carboxylate, [(3R)-1-(tert-butoxycarbonyl)pyrrolidin-3-yl]methanaminium, [(3S)-1-(tert-butoxycarbonyl)pyrrolidin-3-yl]methanaminium, (R)-3-(Aminomethyl)-N-Boc pyrrolidine, 3-Aminomethyl-Pyrrolidine-1-Carboxylic Acid Tert-Butyl Ester,  1-Boc-3-(aminomethyl)-pyrrolidine

3-(Aminomethyl)pyrrolidine, N1-BOC protected

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CAS 270912-72-6: 1-Boc-3-(aminomethyl)pyrrolidine

3-(Aminomethyl)pyrrolidine, N1-BOC protected

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3-Aminomethylpyrrolidine-1-carboxylic acid tert-butyl ester

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3-(Aminomethyl)-1-N-Boc-pyrrolidine

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