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Structure of 711017-85-5
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Boc-(2S)-Gly-4-pyranoyl serves as a specialized amino acid derivative featuring a pyranoyl-protected glycinyl moiety, enabling selective incorporation into peptide chains under mild deprotection conditions. This scaffold offers enhanced stability and solubility in organic solvents, facilitating efficient coupling reactions in complex peptide syntheses.
Boc-(2S)-Gly-4-pyranoyl serves as a versatile chiral building block for the synthesis of glycosylated heterocycles and peptide mimetics. The Boc-protected glycine moiety enables straightforward deprotection and coupling, while the 4-pyranoyl group provides a stable, electron-rich scaffold for subsequent functionalization. Its stereo-defined (2S) configuration ensures predictable reactivity in asymmetric synthesis, and the structure exhibits excellent bench stability and compatibility with standard peptide coupling 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-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: