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CAS 108612-54-0

:

4-N-Boc-4-N-Methyl-aminopiperidine

Description:
4-N-Boc-4-N-Methyl-aminopiperidine, with the CAS number 108612-54-0, is a chemical compound characterized by its piperidine structure, which includes a tert-butoxycarbonyl (Boc) protecting group and a methylamine substituent. This compound is typically utilized in organic synthesis, particularly in the development of pharmaceuticals and biologically active molecules. The Boc group serves as a protective group for amines, allowing for selective reactions without interfering with the amine functionality. The presence of the methyl group enhances the steric and electronic properties of the piperidine ring, potentially influencing its reactivity and interaction with biological targets. 4-N-Boc-4-N-Methyl-aminopiperidine is generally a solid at room temperature and may exhibit solubility in organic solvents. Its stability and reactivity can be affected by factors such as pH and the presence of other functional groups in a synthetic pathway. As with many chemical substances, proper handling and safety precautions are essential due to potential hazards associated with its use.
Formula:C11H22N2O2
InChI:InChI=1/C11H22N2O2/c1-11(2,3)15-10(14)13(4)9-5-7-12-8-6-9/h9,12H,5-8H2,1-4H3
SMILES:CC(C)(C)OC(=O)N(C)C1CCNCC1
Synonyms:
  • Methyl-Piperidin-4-Yl-Carbamic Acid Tert-Butyl Ester
  • Buttpark 90\06-17
  • 4-(Methylamino)piperidine, N4-BOC protected
  • 4-Boc-4-methylaminopiperidine
  • 4-Boc-methylaminopiperidine
  • Tert-Butyl Methyl(Piperidin-4-Yl)Carbamate
  • tert-Butyl N-methyl-N-(4-piperidyl)carbamate
  • tert-butyl Piperidin-4-ylmethylcarbamate
  • 2-Methyl-2-propanyl methyl(4-piperidinyl)carbamate
  • 4-Aminopiperidine-N-Methyl, N-Boc Protected
  • tert-butyl N-methyl-N-(piperidin-4-yl)carbamate
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