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CAS 329910-39-6

:

(1S,3S)-N-BOC-1-Aminocyclopentane-3-carboxylic acid methyl ester

Description:
(1S,3S)-N-BOC-1-Aminocyclopentane-3-carboxylic acid methyl ester is a chemical compound characterized by its bicyclic structure, which includes a cyclopentane ring. The "N-BOC" designation indicates the presence of a tert-butyloxycarbonyl (BOC) protecting group on the amine, which is commonly used in peptide synthesis to protect amino groups. This compound features both an amino group and a carboxylic acid moiety, making it an amino acid derivative. The methyl ester functionality suggests that the carboxylic acid is esterified with methanol, enhancing its solubility and reactivity in various chemical reactions. The specific stereochemistry, denoted by (1S,3S), indicates the spatial arrangement of the substituents around the chiral centers, which is crucial for the compound's biological activity and interaction with enzymes or receptors. Overall, this compound is of interest in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals and biologically active molecules.
Formula:C12H21NO4
InChI:InChI=1/C12H21NO4/c1-12(2,3)17-11(15)13-9-6-5-8(7-9)10(14)16-4/h8-9H,5-7H2,1-4H3,(H,13,15)/t8-,9-/m0/s1
SMILES:CC(C)(C)OC(=N[C@H]1CC[C@@H](C1)C(=O)OC)O
Synonyms:
  • (1S,3S)-N-tert-Butoxycarbonyl-1-aminocyclopentane-3-carboxylic acid methyl ester
  • methyl (1S,3S)-3-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylate
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