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CAS 926906-42-5

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1,1-Dimethylethyl 3-(4-piperidinyloxy)-1-azetidinecarboxylate

Description:
1,1-Dimethylethyl 3-(4-piperidinyloxy)-1-azetidinecarboxylate, identified by its CAS number 926906-42-5, is a chemical compound that features a unique structure combining an azetidine ring with a piperidine moiety. This compound is characterized by the presence of a tert-butyl group (1,1-dimethylethyl) which contributes to its steric bulk and may influence its reactivity and solubility. The piperidinyloxy group suggests potential applications in medicinal chemistry, particularly in the development of pharmacologically active agents. The azetidine ring is a four-membered cyclic amine, which can impart specific biological activities. The ester functional group in the molecule indicates that it may undergo hydrolysis, making it relevant in various chemical reactions. Overall, this compound's structural features suggest it could be of interest in research areas such as drug design and synthesis, particularly for compounds targeting neurological or muscular systems. Its specific properties, such as solubility and stability, would depend on the surrounding conditions and the presence of other functional groups.
Formula:C13H24N2O3
InChI:InChI=1S/C13H24N2O3/c1-13(2,3)18-12(16)15-8-11(9-15)17-10-4-6-14-7-5-10/h10-11,14H,4-9H2,1-3H3
InChI key:InChIKey=SJIOEXVHZCHRRZ-UHFFFAOYSA-N
SMILES:C(OC(C)(C)C)(=O)N1CC(OC2CCNCC2)C1
Synonyms:
  • tert-Butyl 3-[(piperidin-4-yl)oxy]azetidine-1-carboxylate
  • 1-Azetidinecarboxylic acid, 3-(4-piperidinyloxy)-, 1,1-dimethylethyl ester
  • tert-Butyl 3-(4-piperidyloxy)azetidine-1-carboxylate
  • 1,1-Dimethylethyl 3-(4-piperidinyloxy)-1-azetidinecarboxylate
  • tert-butyl 3-(piperidin-4-yloxy)azetidine-1-carboxylate
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