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Structure of 285996-74-9
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This fluorenylmethoxycarbonyl-protected amino ketone integrates seamlessly into peptide synthesis workflows, offering a stable, moisture-tolerant scaffold for late-stage functionalization. The cyclohexanone core enables selective derivatization while the Fmoc group ensures efficient orthogonal deprotection under mild conditions.
1-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-oxocyclohexane-1-carboxylic acid serves as a versatile protected amino carbonyl building block, enabling efficient synthesis of cyclohexanone-derived scaffolds. The Fmoc group provides excellent stability and orthogonal deprotection under mild basic conditions, while the 4-oxo functionality supports downstream transformations including enolization, condensation, and reductive amination. Ideal for peptide and medicinal chemistry applications requiring bench-stable, functionally rich intermediates.
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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-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: