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Structure of 2227199-12-2
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tert-Butyl cis-N-(4-amino-1-methyl-cyclohexyl)carbamate hydrochloride features a sterically hindered cyclohexyl scaffold with a strategically positioned amino group and electron-rich amine functionality. This bench-stable derivative enables direct incorporation into peptide conjugation workflows, offering enhanced solubility in aqueous-organic mixtures while maintaining structural integrity under standard handling conditions.
tert-Butyl cis-N-(4-amino-1-methyl-cyclohexyl)carbamate hydrochloride serves as a versatile building block for the synthesis of substituted cyclohexylamine derivatives. The protected amine and tertiary alcohol functionalities enable orthogonal transformations, while the hydrochloride salt enhances solubility and stability in aqueous and polar organic media. Its cis-configured ring system provides defined stereochemistry for applications in medicinal chemistry and heterocyclic scaffold construction.
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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: