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CAS 155905-78-5

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Cyclobutaneacetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (R)-

Description:
Cyclobutaneacetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (R)- is a chiral compound characterized by its cyclobutane ring structure, which contributes to its unique chemical properties. This substance features an acetic acid moiety, indicating it has acidic characteristics, and an amino group that suggests potential for forming hydrogen bonds and participating in various chemical reactions. The presence of the 1,1-dimethylethoxycarbonyl group enhances its stability and solubility in organic solvents. As a chiral molecule, it exists in two enantiomeric forms, with the (R)- configuration being one of them, which can influence its biological activity and interactions with other molecules. This compound may be of interest in pharmaceutical applications due to its structural features that could affect its reactivity and biological properties. Overall, its unique combination of functional groups and stereochemistry makes it a subject of interest in organic synthesis and medicinal chemistry.
Formula:C11H19NO4
InChI:InChI=1S/C11H19NO4/c1-11(2,3)16-10(15)12-8(9(13)14)7-5-4-6-7/h7-8H,4-6H2,1-3H3,(H,12,15)(H,13,14)/t8-/m1/s1
InChI key:InChIKey=OHDFGIXTRBDGRB-MRVPVSSYSA-N
SMILES:[C@H](NC(OC(C)(C)C)=O)(C(O)=O)[C@@H]1CCC1
Synonyms:
  • (2R)-2-[[(tert-Butoxy)carbonyl]amino]-2-cyclobutylacetic acid
  • (R)-2-((tert-Butoxycarbonyl)amino)-2-cyclobutylacetic acid
  • (R)-2-((tert-Butoxycarbonyl)amino)-2-cyclobutylaceticacid
  • (R)-Tert-Butoxycarbonylamino-Cyclobutyl-Acetic Acid
  • Boc-(2R)-Gly(2-Cyclobutyl)
  • Boc-(R)-2-Cyclobutylglycine
  • Boc-D-Cyclobutyl Glycine
  • Boc-D-Cyclobutylglycine 98%
  • Cyclobutaneacetic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (R)-
  • N-Boc-R-Cyclobutylglycine
  • See more synonyms
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