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CAS 162167-97-7

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3-Aminomethyl-1-N-Boc-piperidine

Description:
3-Aminomethyl-1-N-Boc-piperidine is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated heterocycle containing one nitrogen atom. The "N-Boc" designation indicates that the nitrogen atom is protected by a tert-butyloxycarbonyl (Boc) group, a common protective group used in organic synthesis to prevent unwanted reactions at the amine site. This compound features an aminomethyl substituent at the 3-position of the piperidine ring, which enhances its reactivity and potential applications in medicinal chemistry. It is typically a white to off-white solid and is soluble in organic solvents. The presence of the Boc group allows for selective deprotection under mild acidic conditions, facilitating further functionalization of the amine. 3-Aminomethyl-1-N-Boc-piperidine is often utilized as an intermediate in the synthesis of various pharmaceuticals and biologically active compounds, making it valuable in drug discovery and development. Its properties and reactivity make it a versatile building block in organic synthesis.
Formula:C11H23N2O2
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/p+1/t9-/m0/s1
Synonyms:
  • 1-Boc-3-Aminomethylpiperidine
  • 1-Piperidinecarboxylic Acid, 3-(Aminomethyl)-, 1,1-Dimethylethyl Ester
  • (+/-)-1-N-Boc-Piperidine-3-Methylamine
  • 1-N-Boc-3-(Aminomethyl)-Piperidine
  • 3-(Aminomethyl)-N-Boc-Piperidine
  • Dl-3-Aminomethyl-1-N-Boc-Piperidine
  • Boc-((R,S)-3-Aminomethyl)-Piperidine
  • Tert-Butyl 3-(Aminomethyl)Piperidine-1-Carboxylate
  • [(3R)-1-(tert-butoxycarbonyl)piperidin-3-yl]methanaminium
  • [(3S)-1-(tert-butoxycarbonyl)piperidin-3-yl]methanaminium
  • 3-Aminomethyl-Piperidine-1-Carboxylic Acid Tert-Butyl Ester
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