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Structure of 1400264-85-8
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tert-Butyl 3,3-difluoro-4-oxopiperidine-1-carboxylate hydrate features a sterically hindered piperidine core with dual fluorine atoms at the 3-position, enhancing metabolic stability and modulating electronic properties. The hydrate form ensures improved handling and solubility in aqueous-based reaction systems. This bench-stable intermediate integrates readily into diverse synthetic pathways for bioactive molecule construction.
tert-Butyl 3,3-difluoro-4-oxopiperidine-1-carboxylate hydrate serves as a versatile building block in medicinal chemistry, enabling the construction of fluorinated piperidine scaffolds prevalent in bioactive molecules. The difluoro substitution at C3 enhances metabolic stability and modulates electronic properties, while the 4-oxo functionality supports diverse transformations including reductive amination and nucleophilic addition. Bench-stable and readily purified by standard chromatography, it functions effectively in multistep syntheses requiring robust functional group tolerance.
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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 : H302-H315-H320-H335
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: