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CAS 158567-91-0

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(2R,4R)-1-tert-butoxycarbonyl-4-phenyl-pyrrolidine-2-carboxylic acid

Description:
(2R,4R)-1-tert-butoxycarbonyl-4-phenyl-pyrrolidine-2-carboxylic acid is a chiral compound characterized by its pyrrolidine ring structure, which features a tert-butoxycarbonyl (Boc) protecting group and a phenyl substituent. This compound is typically used in organic synthesis, particularly in the preparation of peptides and other complex molecules due to its ability to protect functional groups during chemical reactions. The presence of the carboxylic acid functional group indicates that it can participate in acid-base reactions and can be involved in esterification or amidation processes. Its chirality, denoted by the (2R,4R) configuration, is crucial for its biological activity, as stereochemistry can significantly influence the interaction of the molecule with biological targets. The compound is likely to be solid at room temperature and may exhibit moderate solubility in organic solvents. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken during use.
Formula:C16H21NO4
InChI:InChI=1/C16H21NO4/c1-16(2,3)21-15(20)17-10-12(9-13(17)14(18)19)11-7-5-4-6-8-11/h4-8,12-13H,9-10H2,1-3H3,(H,18,19)/t12-,13+/m0/s1
Synonyms:
  • (4R)-1-(tert-Butoxycarbonyl)-4-phenyl-D-proline
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