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CAS 915226-39-0

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(S)-1-N-Boc-3-cyanopiperidine

Description:
(S)-1-N-Boc-3-cyanopiperidine is a chiral chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The "N-Boc" designation indicates the presence of a tert-butyloxycarbonyl (Boc) protecting group on the nitrogen atom, which is commonly used in organic synthesis to protect amines. The "3-cyano" part of the name signifies that a cyano group (-C≡N) is attached to the third carbon of the piperidine ring, contributing to the compound's reactivity and potential applications in medicinal chemistry. This compound is typically used as an intermediate in the synthesis of various pharmaceuticals and bioactive molecules due to its unique structural features. Its chirality, indicated by the "(S)" prefix, suggests that it may exhibit specific biological activity or selectivity, making it of interest in drug development. As with many chemical substances, proper handling and safety precautions are essential due to potential toxicity or reactivity.
Formula:C11H18N2O2
InChI:InChI=1/C11H18N2O2/c1-11(2,3)15-10(14)13-6-4-5-9(7-12)8-13/h9H,4-6,8H2,1-3H3/t9-/m1/s1
SMILES:CC(C)(C)OC(=O)N1CCC[C@H](C#N)C1
Synonyms:
  • (S)-3-Cyanopiperidine-1-carboxylic acid tert-butyl ester
  • tert-butyl (3S)-3-cyanopiperidine-1-carboxylate
  • tert-Butyl (S)-3-cyanopiperidine-1-carboxylate
  • (S)-1-N-Boc-3-cyanopiperidine
  • 1-Piperidinecarboxylic acid, 3-cyano-, 1,1-dimethylethyl ester, (3S)-
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