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CAS 135042-17-0

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N-Boc-Trans-4-Hydroxy-D-Proline Methyl Ester

Description:
N-Boc-Trans-4-Hydroxy-D-Proline Methyl Ester is a chemical compound characterized by its structure, which includes a Boc (tert-butyloxycarbonyl) protecting group, a trans-4-hydroxy configuration, and a methyl ester functional group. This compound is a derivative of proline, an amino acid, and is often utilized in peptide synthesis and medicinal chemistry due to its ability to serve as a chiral building block. The Boc group provides stability and protection to the amine during synthetic procedures, while the hydroxyl group can participate in various chemical reactions, including esterification and coupling reactions. The methyl ester functionality enhances solubility and reactivity, making it suitable for further modifications. N-Boc-Trans-4-Hydroxy-D-Proline Methyl Ester is typically a white to off-white solid and is soluble in organic solvents such as methanol and dichloromethane. Its unique stereochemistry and functional groups make it valuable in the development of pharmaceuticals and biologically active compounds.
Formula:C11H19NO5
InChI:InChI=1/C11H19NO5/c1-11(2,3)17-10(15)12-6-7(13)5-8(12)9(14)16-4/h7-8,13H,5-6H2,1-4H3/t7-,8+/m0/s1
Synonyms:
  • 1,2-pyrrolidinedicarboxylic acid, 4-hydroxy-, 1-(1,1-dimethylethyl) 2-methyl ester, (2R,4S)-
  • 1-tert-Butyl 2-methyl (2R,4S)-4-hydroxypyrrolidine-1,2-dicarboxylate
  • (2R,4S)-1-tert-butyl 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate
  • (2S,4R)-1-tert-butyl 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate
  • N-Boc-trans-4-Hydroxy-D-prolinemethyl ester
  • Boc-trans-D-Hyp-Ome
  • Boc-D-trans-Hyp-OMe
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