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CAS 1434142-05-8

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

Description:
Trans-3-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclobutaneacetic acid is a chemical compound characterized by its unique structural features, which include a cyclobutane ring and an amino acid functional group. The presence of the 1,1-dimethylethoxycarbonyl group contributes to its stability and solubility properties. This compound is likely to exhibit both polar and non-polar characteristics due to the combination of its hydrophobic cyclobutane structure and the polar carboxylic acid and amine functionalities. Its stereochemistry, indicated by the "trans" configuration, suggests specific spatial arrangements that can influence its biological activity and interactions. Such compounds may be of interest in pharmaceutical research, particularly in the development of novel therapeutic agents. Additionally, the presence of functional groups allows for potential reactivity in various chemical reactions, making it a versatile candidate for further synthetic modifications. Overall, trans-3-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclobutaneacetic acid represents a complex molecule with potential applications in medicinal chemistry and organic synthesis.
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-ZKCHVHJHNA-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]-, trans-
  • trans-3-[[(1,1-Dimethylethoxy)carbonyl]amino]cyclobutaneacetic acid
  • 2-(trans-3-((tert-Butoxycarbonyl)amino)cyclobutyl)acetic acid
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