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CAS 132945-78-9

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(S)-1-BOC-3-Cyanopyrrolidine

Description:
(S)-1-BOC-3-Cyanopyrrolidine is a chiral compound characterized by its pyrrolidine ring structure, which is a five-membered nitrogen-containing heterocycle. The "BOC" (tert-butyloxycarbonyl) group serves as a protective group for the amine, enhancing the compound's stability and facilitating its use in various synthetic applications, particularly in peptide synthesis. The presence of the cyano group (-C≡N) at the 3-position of the pyrrolidine ring introduces a polar functional group, which can influence the compound's reactivity and solubility. This compound is typically utilized in organic synthesis and medicinal chemistry, where its chirality can be crucial for biological activity. Additionally, (S)-1-BOC-3-Cyanopyrrolidine may exhibit specific stereochemical properties that can affect its interaction with biological targets, making it of interest in drug development. Overall, its unique structural features and functional groups make it a valuable intermediate in the synthesis of more complex molecules.
Formula:C10H16N2O2
InChI:InChI=1/C10H16N2O2/c1-10(2,3)14-9(13)12-5-4-8(6-11)7-12/h8H,4-5,7H2,1-3H3/t8-/m1/s1
SMILES:CC(C)(C)OC(=O)N1CC[C@H](C#N)C1
Synonyms:
  • (S)-1-N-(tert-Butoxycarbonyl)-3-cyanopyrrolidine
  • (S)-1-N-Boc-3-Cyano-Pyrrolidine
  • (S)-3-Cyano-Pyrrolidine-1-Carboxylic Acid Tert-Butyl Ester
  • (S)-Tert-Butyl-3-Cyanopyrrolidine-1-Carboxylate
  • N-T-Boc-3(S)-Cyanopyrrolidine
  • tert-butyl (3S)-3-cyanopyrrolidine-1-carboxylate
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