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Structure of 894096-02-7
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Me-triacetyl-β-D-glucopyranuronate-Ph-CH2OH-Fmoc features a protected glucuronic acid scaffold with a benzyl alcohol handle and Fmoc-blocking group, enabling direct conjugation in glycochemistry workflows. This stable, moisture-tolerant derivative simplifies the synthesis of complex glycoconjugates and oligosaccharide libraries under standard conditions.
Me-triacetyl-β-D-glucopyranuronate-Ph-CH2OH-Fmoc serves as a versatile glycosyl building block for the synthesis of complex oligosaccharides and glycoconjugates. The triacetylated glucuronic acid moiety provides enhanced stability and facilitates selective deprotection, while the Fmoc-protected benzyl alcohol functionality enables orthogonal coupling in solid-phase glycosylation workflows. This construct supports efficient C-glycoside formation and is compatible with standard peptide and carbohydrate 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: