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Structure of 71239-85-5
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N-Boc-3-(2-pyridyl)-L-alanine features a pyridyl-bearing side chain enabling direct incorporation into peptide architectures. The Boc group provides reliable protection of the α-amino functionality, offering stability during storage and handling. This derivative integrates seamlessly into synthetic sequences requiring electron-deficient heteroaromatic motifs.
N-Boc-3-(2-pyridyl)-L-alanine serves as a versatile building block for the synthesis of bioactive peptides and heterocyclic scaffolds. The Boc group provides excellent stability and ease of removal under mild acidic conditions, while the 2-pyridyl moiety offers a handle for metal-catalyzed coupling reactions and enhanced solubility. This amino acid derivative exhibits robust functional group tolerance and is well-suited for solid-phase peptide synthesis and medicinal chemistry campaigns requiring pyridyl-containing analogs.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352
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Lot numbers can be found on the outside label of a product: