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Structure of 197229-63-3
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tert-Butyl (2-oxo-1,2-dihydropyridin-3-yl)carbamate serves as a bench-stable, moisture-tolerant protecting group for pyridine-based intermediates. This carbamate derivative integrates seamlessly into late-stage functionalization workflows, enabling selective transformations at the 3-position of dihydropyridine scaffolds. The tert-butyl moiety enhances solubility and simplifies purification, while the electron-deficient pyridine ring facilitates directed metallation and cross-coupling reactions.
tert-Butyl (2-oxo-1,2-dihydropyridin-3-yl)carbamate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to pyridine-based scaffolds through selective reduction and functionalization. The carbamate group provides excellent stability and facilitates purification, while the 2-oxo functionality supports diverse transformations including nucleophilic addition and cyclization reactions. This reagent functions effectively in standard bench-scale protocols, offering reliable performance in the synthesis of heterocyclic intermediates and medicinal chemistry candidates.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: