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Structure of 31972-52-8
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Boc-Gly-Gly-OH serves as a key dipeptide building block in peptide synthesis, featuring a stable tert-butoxycarbonyl (Boc) protecting group at the N-terminus and a free C-terminal carboxylic acid. This configuration enables straightforward coupling reactions under standard conditions, with the Boc moiety readily removed via mild acidolysis to reveal the active amine for further elongation. The molecule exhibits excellent bench stability and solubility in common organic solvents, facilitating use in both solution-phase and solid-phase workflows.
Boc-Gly-Gly-OH serves as a reliable dipeptide building block for peptide synthesis, offering bench-stable protection of the N-terminus via the Boc group and a free C-terminal carboxylic acid. Its orthogonal functionality enables straightforward coupling reactions in solid-phase and solution-phase workflows, with high purity and consistent reactivity across standard amide bond formation protocols.
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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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: