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Structure of 347186-01-0
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tert-Butyl N-(3-aminocyclohexyl)carbamate features a protected amine on a cyclohexyl scaffold, enabling stable incorporation into multi-step syntheses. The tert-butyl carbamate group facilitates selective deprotection under mild acidic conditions, while the secondary amine supports efficient coupling reactions. This derivative offers enhanced solubility and handling stability in organic synthesis workflows.
tert-Butyl N-(3-aminocyclohexyl)carbamate serves as a stable, bench-friendly amino protecting group variant, enabling selective functionalization at the primary amine. Its cyclohexyl scaffold provides conformational rigidity useful in medicinal chemistry lead optimization. The tert-butyl carbamate (Boc) moiety facilitates mild acid cleavage under standard conditions, allowing straightforward deprotection during late-stage synthesis. This compound functions reliably in multi-step sequences requiring orthogonal protection strategies and demonstrates excellent compatibility with diverse reaction conditions.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: