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CAS 1402714-51-5

:

3-Quinolineacetic acid, 4-(2,3-dihydropyrano[4,3,2-de]quinolin-7-yl)-α-(1,1-dimethylethoxy)-2-methyl-, methyl ester, (αS,4R)-

Description:
3-Quinolineacetic acid, 4-(2,3-dihydropyrano[4,3,2-de]quinolin-7-yl)-α-(1,1-dimethylethoxy)-2-methyl-, methyl ester, with the CAS number 1402714-51-5, is a complex organic compound characterized by its quinoline and pyran structural motifs. This compound features a quinoline backbone, which is known for its aromatic properties and biological activity, particularly in medicinal chemistry. The presence of the dihydropyrano group adds to its structural diversity and may influence its reactivity and interaction with biological targets. The α-(1,1-dimethylethoxy) group suggests steric hindrance, which can affect the compound's solubility and permeability. As a methyl ester, it is likely to exhibit different solubility characteristics compared to its acid form, potentially enhancing its bioavailability. The specific stereochemistry indicated by (αS,4R) suggests that the compound may exhibit chirality, which can significantly impact its pharmacological properties. Overall, this compound's unique structure may confer interesting biological activities, making it a subject of interest in pharmaceutical research.
Formula:C28H28N2O4
Synonyms:
  • 3-Quinolineacetic acid, 4-(2,3-dihydropyrano[4,3,2-de]quinolin-7-yl)-α-(1,1-dimethylethoxy)-2-methyl-, methyl ester, (αS,4R)-
  • (S)-methyl 2-(tert-butoxy)-2-((R)-4-(2,3-dihydropyrano[4,3,2-de]quinolin-7-yl)-2-methylquinolin-3-yl)acetate
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