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Structure of 32384-65-9
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This tetrahydro-pyranone derivative features four trimethylsilyl ether groups that confer exceptional stability and solubility in organic media. The protected hydroxyl functionalities enable reliable use in multistep carbohydrate synthesis, where the silyl moieties serve as orthogonal masking groups. This compound functions as a key building block for complex glycosyl donors and advanced oligosaccharide assembly.
(3R,4S,5R,6R)-3,4,5-Tris((trimethylsilyl)oxy)-6-(((trimethylsilyl)oxy)methyl)tetrahydro-2H-pyran-2-one serves as a highly functionalized glycal equivalent, enabling efficient access to complex oligosaccharide building blocks. Its multiple silyl ether groups confer excellent bench stability and orthogonal deprotection profiles, facilitating sequential transformations in stereoselective glycosylation workflows. The C6 aldehyde functionality reacts readily with nucleophiles under mild conditions, while the protected hydroxyls tolerate a broad range of reaction conditions, making it a versatile scaffold for carbohydrate synthesis and natural product derivatization.
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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: