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CAS 141774-70-1

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(S)-2-N-BOC-Aminomethylpyrrolidine

Description:
(S)-2-N-BOC-Aminomethylpyrrolidine is a chiral compound characterized by its pyrrolidine ring structure, which is a five-membered nitrogen-containing heterocycle. The "N-BOC" designation indicates that the amine group 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 is typically utilized in the synthesis of pharmaceuticals and biologically active molecules due to its ability to serve as a building block in the formation of more complex structures. Its chirality, denoted by the (S) configuration, is significant in medicinal chemistry, as the specific stereochemistry can influence the biological activity and pharmacokinetics of the resulting compounds. The presence of the aminomethyl group enhances its reactivity, making it a versatile intermediate in various chemical reactions. Overall, (S)-2-N-BOC-Aminomethylpyrrolidine is valued for its functional groups and stereochemical properties, which are essential in the development of new therapeutic agents.
Formula:C10H20N2O2
InChI:InChI=1/C10H20N2O2/c1-10(2,3)14-9(13)12-7-8-5-4-6-11-8/h8,11H,4-7H2,1-3H3,(H,12,13)/t8-/m0/s1
SMILES:CC(C)(C)OC(=NC[C@@H]1CCCN1)O
Synonyms:
  • S-2-(BOC-Aminomethyl)Pyrrolidine
  • (S)-Pyrrolidin-2-ylmethyl-Carbamic acid Tert-butyl ester
  • tert-butyl [(2S)-pyrrolidin-2-ylmethyl]carbamate
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