CymitQuimica logo

CAS 706806-60-2

:

2-benzyl-1-(tert-butoxycarbonyl)-L-proline

Description:
2-benzyl-1-(tert-butoxycarbonyl)-L-proline is an amino acid derivative characterized by its unique structural features, which include a proline backbone modified with a benzyl group and a tert-butoxycarbonyl (Boc) protecting group. The presence of the benzyl group enhances lipophilicity, potentially influencing its solubility and reactivity in organic solvents. The Boc group serves as a protective moiety for the amino group, making it useful in peptide synthesis and other organic reactions where selective deprotection is required. This compound is typically utilized in the synthesis of peptides and other bioactive molecules due to its ability to participate in various coupling reactions. Its chirality, stemming from the L-proline configuration, is significant in biological contexts, as it can affect the compound's interaction with biological targets. Overall, 2-benzyl-1-(tert-butoxycarbonyl)-L-proline is a valuable intermediate in organic synthesis, particularly in the field of medicinal chemistry and drug development.
Formula:C17H23NO4
InChI:InChI=1/C17H23NO4/c1-16(2,3)22-15(21)18-11-7-10-17(18,14(19)20)12-13-8-5-4-6-9-13/h4-6,8-9H,7,10-12H2,1-3H3,(H,19,20)/t17-/m1/s1
SMILES:CC(C)(C)OC(=O)N1CCC[C@@]1(Cc1ccccc1)C(=O)O
Synonyms:
  • Boc-(R)-α-benzyl-Pro-OH, CAS 706806-60-2
  • 1,2-Pyrrolidinedicarboxylic acid, 2-(phenylmethyl)-, 1-(1,1-dimethylethyl) ester, (2R)-
  • (R)-2-Benzyl-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic aci
  • BOC-(R)-ALPHA-BENZYL-PROLINE USP/EP/BP
  • BOC-(R)-ALPHA-BENZYL-PRO-OH
  • Boc-R-α-Bzl-Pro-OH
  • BOC-ALPHA-BENZYL L-PROLINE
  • 2-Benzyl-N-Boc-L-proline, 95%
  • (R)-2-benzyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester
  • See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.