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CAS 140645-23-4

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(R)-N-Boc-3-aminomethylpiperidine

Description:
(R)-N-Boc-3-aminomethylpiperidine is a chiral amine compound characterized by its piperidine ring structure, which includes a tert-butyloxycarbonyl (Boc) protecting group on the nitrogen atom. This compound is notable for its application in organic synthesis, particularly in the development of pharmaceuticals and biologically active molecules. The presence of the Boc group enhances the stability and solubility of the amine, facilitating its use in various chemical reactions. The (R) configuration indicates the specific stereochemistry of the molecule, which is crucial for its biological activity and interaction with other chiral substances. Additionally, the aminomethyl substituent at the 3-position of the piperidine ring contributes to its reactivity and potential as a building block in synthetic pathways. Overall, (R)-N-Boc-3-aminomethylpiperidine is valued for its versatility in synthetic chemistry and its role in the design of chiral compounds.
Formula:C11H22N2O2
InChI:InChI=1/C11H22N2O2/c1-11(2,3)15-10(14)13-6-4-5-9(7-12)8-13/h9H,4-8,12H2,1-3H3
SMILES:CC(C)(C)OC(=O)N1CCCC(CN)C1
Synonyms:
  • (R)-3-Aminomethyl-Piperidine-1-Carboxylic Acid Tert-Butyl Ester
  • (R)-3-Aminomethyl-1-N-Boc-Piperidine
  • (R)-1-N-Boc-3-(Aminomethyl)Piperidine
  • (R)-1-N-Boc-Piperidine-3-Methylamine
  • (R)-1-Boc-3-(Aminomethyl)Piperidine
  • (R)-Tert-Butyl 3-(Aminomethyl)Piperidine-1-Carboxylate
  • 1,1-dimethyl (3R)-3-(aminomethyl)-1-piperidinecarboxylate
  • tert-butyl (3R)-3-(aminomethyl)piperidine-1-carboxylate
  • Tert-Butyl 3-(Aminomethyl)Piperidine-1-Carboxylate
  • (R)-3-(Aminomethyl)-1-Boc-piperidine
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