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Structure of 35264-05-2
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This cyclohexyl-substituted amino acid derivative features a tert-butoxycarbonyl-protected amine, enabling stable incorporation into peptide synthesis workflows. The hydrophobic cyclohexyl moiety enhances membrane permeability, while the carboxylic acid group facilitates conjugation. Designed for modular assembly in bioactive molecule construction.
2-((tert-Butoxycarbonyl)amino)-2-cyclohexylacetic acid serves as a versatile building block for the synthesis of bioactive peptides and heterocyclic scaffolds. The Boc-protected amino group enables facile deprotection under mild acidic conditions, while the cyclohexylacetic acid moiety provides steric bulk and metabolic stability. This compound exhibits excellent bench stability, tolerates diverse reaction conditions, and facilitates purification via standard chromatographic methods. Its structure supports use in solid-phase peptide synthesis and as a precursor to cyclic amides and other medicinally relevant architectures.
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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: