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Structure of 1350734-61-0
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(3R,4R)-3-Aminotetrahydro-2H-pyran-4-ol features a stereochemically defined pyran ring with adjacent amine and hydroxyl groups, enabling precise incorporation into chiral synthetic intermediates. This bench-stable scaffold delivers high diastereoselectivity in glycosylation and cyclization reactions, supporting efficient access to complex carbohydrate architectures and bioactive heterocycles under standard conditions.
(3R,4R)-3-Aminotetrahydro-2H-pyran-4-ol serves as a valuable chiral building block in medicinal chemistry, enabling efficient access to tetrahydropyran-containing scaffolds prevalent in bioactive molecules. Its well-defined stereochemistry and complementary functional groups—primary amine and secondary alcohol—facilitate selective transformations, including amide coupling, protection sequences, and cyclization reactions. The compound exhibits excellent bench stability and is readily purified by standard techniques, supporting its use in both small-molecule synthesis and process development 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: