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CAS 334769-80-1

:

(2S,5S)-N-Boc-5-methylpyrrolidine-2-carboxylic acid

Description:
(2S,5S)-N-Boc-5-methylpyrrolidine-2-carboxylic acid is a chiral compound characterized by its pyrrolidine ring structure, which includes a carboxylic acid functional group and a tert-butyloxycarbonyl (Boc) protecting group on the nitrogen atom. This compound is typically used in organic synthesis, particularly in the preparation of peptides and other biologically active molecules due to its ability to serve as a building block. The presence of the Boc group provides stability and protects the amine during various chemical reactions, while the carboxylic acid group can participate in coupling reactions. The specific stereochemistry, indicated by the (2S,5S) configuration, is crucial for the biological activity and interaction of the compound with other molecules. Additionally, the methyl group at the 5-position contributes to the compound's steric properties, influencing its reactivity and solubility. Overall, this compound is significant in medicinal chemistry and synthetic organic chemistry for its utility in constructing complex molecular architectures.
Formula:C11H19NO4
InChI:InChI=1/C11H19NO4/c1-7-5-6-8(9(13)14)12(7)10(15)16-11(2,3)4/h7-8H,5-6H2,1-4H3,(H,13,14)/t7-,8-/m0/s1
SMILES:C[C@H]1CC[C@@H](C(=O)O)N1C(=O)OC(C)(C)C
Synonyms:
  • (2S,5S)-1-(tert-Butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic acid
  • (2S,5S)-5-Methyl-1,2-pyrrolidinedicarboxylic acid 1-(1,1-dimethylethyl) ester
  • (2S,5S)-1-(tert-Butoxycarbonyl)-5-methyl  pyrrolidine-2-carboxylic  acid
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