Tert-Butyl (3R)-3-(methylamino)piperidine-1-carboxylate is a chemical compound characterized by its piperidine structure, which includes a tert-butyl ester group and a methylamino substituent. This compound features a piperidine ring, a six-membered nitrogen-containing heterocycle, which contributes to its basicity and potential for forming hydrogen bonds. The presence of the tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents, while the carboxylate moiety can participate in various chemical reactions, including esterification and amidation. The methylamino group introduces a secondary amine functionality, which can influence the compound's reactivity and interaction with biological systems. This compound may be of interest in medicinal chemistry for its potential applications in drug development, particularly in the design of compounds targeting specific receptors or enzymes. Its stereochemistry, indicated by the (3R) designation, suggests that it may exhibit specific biological activity based on its three-dimensional conformation. Overall, the unique combination of functional groups and structural features makes this compound a subject of interest in various chemical and pharmaceutical research contexts.

tert-Butyl (3R)-3-(methylamino)piperidine-1-carboxylate

203941-94-0: (R)-1-N-BOC-3-Methylaminopiperidine, R-N-Boc-3-methylamino piperidine, (R)-1-N-BOC-3-Methylamino piperidine

(R)-1-N-Boc-3-Methylamino piperidine

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CAS 203941-94-0: tert-Butyl (3R)-3-(methylamino)piperidine-1-carboxylate

tert-Butyl (3R)-3-(methylamino)piperidine-1-carboxylate

Ref: 54-OR90308

(R)-1-N-Boc-3-Methylamino piperidine

Ref: 10-F048638

(R)-1-N-Boc-3-Methylaminopiperidine

Ref: 3D-FB155108

1-Piperidinecarboxylic acid, 3-(methylamino)-, 1,1-dimethylethyl ester, (3R)-

Ref: IN-DA00297F