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CAS 1256337-02-6

:

6-[[(1,1-Dimethylethoxy)carbonyl]amino]-3-pyridineacetic acid

Description:
6-[[(1,1-Dimethylethoxy)carbonyl]amino]-3-pyridineacetic acid, identified by its CAS number 1256337-02-6, is a chemical compound characterized by its pyridine and acetic acid functional groups. This compound features a pyridine ring substituted at the 3-position with an acetic acid moiety, and at the 6-position, it has an amino group that is further modified by a 1,1-dimethylethoxycarbonyl group. The presence of the dimethylethoxycarbonyl group enhances the compound's stability and solubility, making it suitable for various applications in medicinal chemistry and organic synthesis. The compound is likely to exhibit polar characteristics due to the carboxylic acid and amino functionalities, which can participate in hydrogen bonding. Additionally, its structural features suggest potential biological activity, possibly as a pharmaceutical agent or a precursor in drug development. As with many organic compounds, its reactivity and interactions will depend on the specific conditions and environments in which it is used.
Formula:C12H16N2O4
InChI:InChI=1S/C12H16N2O4/c1-12(2,3)18-11(17)14-9-5-4-8(7-13-9)6-10(15)16/h4-5,7H,6H2,1-3H3,(H,15,16)(H,13,14,17)
InChI key:InChIKey=OXQVDWZWFHQQLU-UHFFFAOYSA-N
SMILES:N(C(OC(C)(C)C)=O)C1=CC=C(CC(O)=O)C=N1
Synonyms:
  • 6-[[(1,1-Dimethylethoxy)carbonyl]amino]-3-pyridineacetic acid
  • (6-tert-Butoxycarbonylamino-pyridin-3-yl)-acetic acid
  • 3-Pyridineacetic acid, 6-[[(1,1-dimethylethoxy)carbonyl]amino]-
  • (6-tert-Butoxycarbonylaminopyridin-3-yl) acetic acid
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