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Structure of 478646-28-5
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Benzyl (R)-(1,5-dihydroxypentan-2-yl)carbamate features a chiral (R)-configured pentanediol backbone with dual hydroxyl groups and a bench-stable benzyl carbamate protecting group. This configuration enables selective glycosylation reactions and facilitates the synthesis of complex oligosaccharides under mild conditions.
Benzyl (R)-(1,5-dihydroxypentan-2-yl)carbamate serves as a chiral auxiliary and protected amino alcohol building block in synthetic organic chemistry. Its orthogonal hydroxyl and carbamate functionalities enable selective transformations in complex molecule assembly. The benzyl group facilitates easy removal under mild hydrogenolysis conditions, while the (R)-stereochemistry ensures predictable stereoselective outcomes in asymmetric synthesis. This compound exhibits excellent bench stability and is compatible with standard purification methods, making it a reliable choice for medicinal chemistry and natural product synthesis workflows.
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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: