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CAS 136315-71-4

:

rel-(1R,2R)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclopentanecarboxylic acid

Description:
Rel-(1R,2R)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclopentanecarboxylic acid, with CAS number 136315-71-4, is a chiral compound characterized by its cyclopentane structure, which features a carboxylic acid functional group and an amino group that is protected by a dimethylethoxycarbonyl (DMEC) moiety. This compound exhibits properties typical of amino acids, including the ability to participate in peptide bond formation, making it relevant in the synthesis of peptides and pharmaceuticals. The presence of the dimethylethoxycarbonyl group provides stability and protection to the amino group during chemical reactions, facilitating selective transformations. Its stereochemistry, denoted by the (1R,2R) configuration, is crucial for its biological activity, as chirality can significantly influence the interaction of the molecule with biological targets. The compound is likely to be soluble in polar solvents due to the presence of the carboxylic acid group, and its solid-state properties may include crystalline formation, which is common for amino acid derivatives. Overall, this compound is of interest in medicinal chemistry and organic synthesis.
Formula:C11H19NO4
InChI:InChI=1/C11H19NO4/c1-11(2,3)16-10(15)12-8-6-4-5-7(8)9(13)14/h7-8H,4-6H2,1-3H3,(H,12,15)(H,13,14)/t7-,8-/s2
InChI key:InChIKey=BUEPEVBYNBQNED-YZYOREDDNA-N
SMILES:C(O)(=O)[C@H]1[C@H](NC(OC(C)(C)C)=O)CCC1
Synonyms:
  • Boc-trans-2-aminocyclopentanecarboxylic acid
  • rel-(1R,2R)-2-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclopentanecarboxylic acid
  • Cyclopentanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, trans-
  • Cyclopentanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, trans-(±)-
  • Cyclopentanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (1R,2R)-rel-
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