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CAS 160033-52-3

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

Description:
(2S,5R)-N-Boc-5-methylpyrrolidine-2-carboxylic acid is a chiral amino acid derivative characterized by its pyrrolidine ring structure, which features a tert-butyloxycarbonyl (Boc) protecting group on the nitrogen atom. This compound is notable for its stereochemistry, with specific configurations at the 2 and 5 positions, contributing to its potential applications in asymmetric synthesis and pharmaceutical development. The presence of the carboxylic acid functional group allows for reactivity typical of amino acids, such as peptide bond formation. The Boc group serves as a protective moiety, facilitating the selective functionalization of the molecule during synthetic processes. This compound is often utilized in the synthesis of more complex molecules, particularly in the field of medicinal chemistry, where the chirality and functional groups can influence biological activity. Its CAS number, 160033-52-3, provides a unique identifier for regulatory and safety information. Overall, (2S,5R)-N-Boc-5-methylpyrrolidine-2-carboxylic acid is a valuable intermediate in organic synthesis and drug development.
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+/m1/s1
Synonyms:
  • (2S,5R)-1-(tert-Butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic acid
  • (2S,5R)-5-Methyl-1,2-pyrrolidinedicarboxylic acid 1-(1,1-dimethylethyl) ester
  • (5R)-1-(tert-butoxycarbonyl)-5-methyl-L-proline
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