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Structure of 1788036-28-1
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tert-Butyl N-[(1S,3S)-3-aminocyclohexyl]carbamate is a bench-stable, chiral building block featuring a protected primary amine on a rigid cyclohexyl scaffold. This configuration enables selective functionalization in asymmetric synthesis and peptide derivatization workflows. The tert-butyl carbamate group facilitates straightforward deprotection under mild acidic conditions, preserving stereochemical integrity during downstream transformations.
tert-Butyl N-[(1S,3S)-3-aminocyclohexyl]carbamate serves as a versatile chiral building block in medicinal chemistry, enabling the construction of cyclohexane-based scaffolds with defined stereochemistry. The tert-butyl carbamate (Boc) group provides excellent bench stability and orthogonal deprotection under mild acidic conditions. The primary amine functionality facilitates straightforward derivatization via amide coupling, reductive amination, or cross-coupling reactions, making it well-suited for modular synthesis workflows in API development.
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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: