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Structure of 915095-99-7
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This tetraacetate derivative features a protected glycosyl scaffold with orthogonal functionalization, enabling selective deprotection and downstream conjugation in complex carbohydrate synthesis. The chlorinated aryl group imparts enhanced lipophilicity and metabolic stability, while the tetrahydrofuran-3-yl ether moiety provides stereochemical control during coupling steps.
(2R,3R,4R,5S,6S)-2-(acetoxymethyl)-6-(4-chloro-3-(4-(((S)-tetrahydrofuran-3-yl)oxy)benzyl)phenyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate serves as a highly functionalized glycosyl donor scaffold, enabling stereoselective glycosylation reactions in complex carbohydrate and glycoconjugate synthesis. The triacetate protection pattern ensures bench stability and facilitates orthogonal deprotection strategies. Its rigid pyran ring framework with multiple chiral centers supports precise stereochemical control in downstream coupling steps.
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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
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: