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CAS 131852-53-4

:

(S)-(-)-1-Benzyl-3-(Boc-Amino)Pyrrolidine

Description:
(S)-(-)-1-Benzyl-3-(Boc-Amino)Pyrrolidine is a chiral organic compound characterized by its pyrrolidine ring, which is a five-membered nitrogen-containing heterocycle. The presence of a benzyl group at the first position and a tert-butoxycarbonyl (Boc) protecting group on the amino group at the third position contributes to its structural complexity and functionality. This compound is often utilized in organic synthesis and medicinal chemistry due to its potential as a building block for more complex molecules, particularly in the development of pharmaceuticals. The Boc group serves as a protective moiety that can be easily removed under acidic conditions, allowing for the selective functionalization of the amino group. The chirality of the compound is significant, as it can influence the biological activity and interaction with biological targets. Its CAS number, 131852-53-4, is a unique identifier that facilitates the search for information regarding its properties, synthesis, and applications in scientific literature. Overall, this compound exemplifies the importance of stereochemistry in the design of biologically active molecules.
Formula:C16H24N2O2
InChI:InChI=1/C16H24N2O2/c1-16(2,3)20-15(19)17-14-9-10-18(12-14)11-13-7-5-4-6-8-13/h4-8,14H,9-12H2,1-3H3,(H,17,19)/t14-/m0/s1
SMILES:CC(C)(C)OC(=N[C@H]1CCN(Cc2ccccc2)C1)O
Synonyms:
  • Tert-Butyl(S)-1-Benzylpyrrolidin-3-Ylcarbamate
  • (S)-1-Benzyl-3-(Tert-Butoxycarbonylamino)Pyrrolidine
  • (S)-N-Benzyl-3-Boc-Amino Pyrrolidine
  • (S)-1-Benzyl-3-N-Boc-Amino-Pyrrolidine
  • (S)-Tert-Butyl 1-Benzylpyrrolidin-3-Ylcarbamate
  • Tert-Butyl [(3S)-1-Benzylpyrrolidin-3-Yl]Carbamate
  • (S)-1-Benzyl-3-(Boc-Amino)Pyrrolidine
  • (S)-(1-Benzyl-pyrrolidin-3-yl)-carbamic acid tert-butyl ester
  • Carbamic acid, N-[(3S)-1-(phenylmethyl)-3-pyrrolidinyl]-, 1,1-dimethylethyl ester
  • (1-Benzyl-pyrrolidin-3-yl)-carbamic acid tert-butyl ester
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