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Structure of 7355-18-2
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Methyl tetra-O-acetyl-β-D-glucopyranuronate features a fully acetylated pyranose ring with β-configuration, offering enhanced stability and solubility in organic solvents. This derivative serves as a protected building block for glycosylation reactions and structural studies of uronic acid-containing polysaccharides.
Methyl tetra-O-acetyl-β-D-glucopyranuronate serves as a key building block in the synthesis of glycosaminoglycans and related carbohydrate-based scaffolds. Its acetylated hydroxyl groups enhance stability and facilitate selective deprotection, enabling controlled glycosylation reactions. The β-configured glucopyranuronate moiety supports reliable stereochemical control in oligosaccharide assembly, making it valuable for synthetic studies requiring precise structural fidelity.
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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: