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CAS 1434141-68-0

:

cis-3-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclobutaneacetic acid

Description:
Cis-3-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclobutaneacetic acid is a chemical compound characterized by its unique structural features, including a cyclobutane ring and an amino acid functional group. The presence of the dimethylethoxycarbonyl moiety suggests that it has protective group characteristics, commonly used in organic synthesis to temporarily mask functional groups. This compound is likely to exhibit properties typical of amino acids, such as the ability to form hydrogen bonds and participate in various chemical reactions, including peptide bond formation. Its cis configuration indicates specific stereochemistry, which can influence its biological activity and interactions with other molecules. The compound may also display solubility in polar solvents due to the presence of the carboxylic acid group, while the cyclobutane structure may contribute to its rigidity and conformational stability. Overall, this compound's characteristics make it of interest in medicinal chemistry and synthetic organic chemistry, particularly in the development of pharmaceuticals or biologically active compounds.
Formula:C11H19NO4
InChI:InChI=1/C11H19NO4/c1-11(2,3)16-10(15)12-8-4-7(5-8)6-9(13)14/h7-8H,4-6H2,1-3H3,(H,12,15)(H,13,14)/t7-,8+
InChI key:InChIKey=FITPVQKCXOGZGO-OCAPTIKFNA-N
SMILES:N(C(OC(C)(C)C)=O)[C@@H]1C[C@H](CC(O)=O)C1
Synonyms:
  • Cyclobutaneacetic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-, cis-
  • cis-3-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclobutaneacetic acid
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