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CAS 174060-98-1

:

(S)-N-Boc-3,3-dimethylpyrrolidine-2-carboxylic acid

Description:
(S)-N-Boc-3,3-dimethylpyrrolidine-2-carboxylic acid is a chiral compound that belongs to the class of pyrrolidine derivatives. It features a tert-butyloxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to protect amines during chemical reactions. The compound has a pyrrolidine ring, which is a five-membered nitrogen-containing heterocycle, and it possesses two methyl groups at the 3-position, contributing to its steric bulk and influencing its reactivity and interactions. The carboxylic acid functional group at the 2-position provides acidic properties, allowing for potential participation in various chemical reactions, such as esterification or amidation. This compound is often utilized in the synthesis of peptides and other biologically active molecules due to its ability to serve as a building block in medicinal chemistry. Its chirality is significant for biological activity, as enantiomers can exhibit different pharmacological effects. Overall, (S)-N-Boc-3,3-dimethylpyrrolidine-2-carboxylic acid is a valuable intermediate in organic synthesis and pharmaceutical development.
Formula:C12H21NO4
InChI:InChI=1/C12H21NO4/c1-11(2,3)17-10(16)13-7-6-12(4,5)8(13)9(14)15/h8H,6-7H2,1-5H3,(H,14,15)/t8-/m1/s1
SMILES:CC(C)(C)OC(=O)N1CCC(C)(C)[C@H]1C(=O)O
Synonyms:
  • Boc-(2S)-3,3-Dimethyl-2-Pyrrolidenecarboxylic Acid
  • (2S)-3,3-Dimethyl-1,2-pyrrolidinedicarboxylic Acid 1-(1,1-Dimethylethyl) Ester
  • (S)-1-(tert-Butoxycarbonyl)-3,3-dimethylpyrrolidine-2-carboxylic acid
  • 1-(tert-butoxycarbonyl)-3,3-dimethyl-L-proline
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