CymitQuimica logo

CAS 161601-29-2

:

(1S,3S)-N-Boc-Aminocyclopentane-3-carboxylic acid

Description:
(1S,3S)-N-Boc-Aminocyclopentane-3-carboxylic acid is a chiral compound characterized by its bicyclic structure, which includes a cyclopentane ring. The "N-Boc" designation indicates that the amine group is protected by a tert-butyloxycarbonyl (Boc) group, a common protecting group in organic synthesis that enhances the stability and reactivity of the amine. This compound features a carboxylic acid functional group, which contributes to its acidity and potential for forming salts. The specific stereochemistry, denoted by (1S,3S), indicates the spatial arrangement of atoms around the chiral centers, which is crucial for its biological activity and interactions. As a building block in peptide synthesis and drug development, this compound may exhibit interesting pharmacological properties. Its solubility, stability, and reactivity can be influenced by the presence of the Boc group and the carboxylic acid, making it a valuable intermediate in organic synthesis and medicinal chemistry.
Formula:C11H18NO4
InChI:InChI=1/C11H19NO4/c1-11(2,3)16-10(15)12-8-5-4-7(6-8)9(13)14/h7-8H,4-6H2,1-3H3,(H,12,15)(H,13,14)/p-1/t7-,8-/m0/s1
SMILES:CC(C)(C)OC(=N[C@H]1CC[C@@H](C1)C(=O)[O-])O
Synonyms:
  • (1S,3S)-3-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylate
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.