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CAS 1799438-98-4

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5-Oxa-2,7-diazaspiro[3.4]octane-2-carboxylic acid, 6-oxo-, 1,1-dimethylethyl ester

Description:
5-Oxa-2,7-diazaspiro[3.4]octane-2-carboxylic acid, 6-oxo-, 1,1-dimethylethyl ester is a chemical compound characterized by its unique spirocyclic structure, which incorporates both nitrogen and oxygen heteroatoms. The presence of the spiro configuration indicates that the molecule contains two rings that share a common atom, contributing to its rigidity and potential biological activity. The carboxylic acid functional group suggests that it can participate in various chemical reactions, such as esterification or amidation. The dimethylethyl ester moiety enhances its lipophilicity, potentially influencing its solubility and permeability in biological systems. This compound may exhibit interesting pharmacological properties due to its structural features, making it a candidate for further research in medicinal chemistry. Its CAS number, 1799438-98-4, allows for precise identification in chemical databases, facilitating studies related to its synthesis, reactivity, and applications in various fields, including pharmaceuticals and agrochemicals. Overall, the compound's unique structure and functional groups suggest a range of potential applications and biological interactions.
Formula:C10H16N2O4
InChI:InChI=1S/C10H16N2O4/c1-9(2,3)16-8(14)12-5-10(6-12)4-11-7(13)15-10/h4-6H2,1-3H3,(H,11,13)
InChI key:InChIKey=MDUVXSNNJOOYHF-UHFFFAOYSA-N
SMILES:C(OC(C)(C)C)(=O)N1CC2(C1)CNC(=O)O2
Synonyms:
  • 1,1-Dimethylethyl 6-oxo-5-oxa-2,7-diazaspiro[3.4]octane-2-carboxylate
  • 5-Oxa-2,7-diazaspiro[3.4]octane-2-carboxylic acid, 6-oxo-, 1,1-dimethylethyl ester
  • tert-Butyl 6-oxo-5-oxa-2,7-diazaspiro[3.4]octane-2-carboxylate
  • 2-Boc-5-oxa-2,7-diazaspiro[3.4]octan-6-one
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