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Structure of 98-53-3
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4-(tert-Butyl)cyclohexanone features a sterically hindered tert-butyl group that imparts enhanced stability and solubility in organic media. This ketone serves as a robust scaffold for asymmetric synthesis, where the bulky substituent directs stereoselective transformations. The conjugated cyclohexanone ring enables efficient functionalization under mild conditions.
4-(tert-Butyl)cyclohexanone serves as a stable, bench-ready ketone scaffold for stereoselective transformations in organic synthesis. Its tertiary butyl group provides steric bulk and enhanced stability, while the cyclohexanone ring enables efficient enolate formation, Michael additions, and reductive amination. The compound functions as a key building block in the construction of complex cyclic frameworks relevant to medicinal chemistry and natural product synthesis.
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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-H412
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Precautionary Statements : P264-P270-P273-P330-P501
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Lot numbers can be found on the outside label of a product: