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CAS 90822-22-3

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(R)-4-nitrobenzyl 4-((2R,3S)-3-((R)-1-((tert-butyldimethylsilyl)oxy)ethyl)-4-oxoazetidin-2-yl)-3-oxopentanoate

Description:
(R)-4-nitrobenzyl 4-((2R,3S)-3-((R)-1-((tert-butyldimethylsilyl)oxy)ethyl)-4-oxoazetidin-2-yl)-3-oxopentanoate, with CAS number 90822-22-3, is a complex organic compound characterized by its multi-functional structure. It features a nitrobenzyl moiety, which contributes to its potential reactivity and solubility properties. The presence of an azetidine ring indicates that it may exhibit unique stereochemical properties, particularly due to the specified (R) and (S) configurations. The tert-butyldimethylsilyl group suggests that the compound may be used in synthetic applications, particularly in protecting groups during organic synthesis. Additionally, the ester functional group in the structure implies that it may participate in hydrolysis reactions, making it relevant in biochemical contexts. Overall, this compound's intricate structure and functional groups suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or as intermediates in organic synthesis. Its specific characteristics would be further elucidated through experimental studies, including its solubility, stability, and reactivity under various conditions.
Formula:C23H34N2O7Si
Synonyms:
  • (R)-4-nitrobenzyl 4-((2R,3S)-3-((R)-1-((tert-butyldimethylsilyl)oxy)ethyl)-4-oxoazetidin-2-yl)-3-oxopentanoate
  • 2-Azetidinebutanoic acid, 3-[(1R)-1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethyl]-γ-methyl-β,4-dioxo-, (4-nitrophenyl)methyl ester, (γR,2R,3S)-
  • Meropenem Impurity 42
  • (3S,4R)-3-<(1R)-1-<(tert-Butyldimethylsilyl)oxy>ethyl>-4-<(1R)-1-methyl-3-(p-nitrobenzyloxycarbonyl)-2-oxopropyl>azetidin-2-one
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