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*For research and further manufacturing use only, not for direct human use.
Structure of 330975-13-8
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rel-(3R,4S)-4-Aminotetrahydrofuran-3-ol is a stereochemically defined heterocyclic amino alcohol featuring a constrained tetrahydrofuran ring with adjacent amine and hydroxyl functionalities. This configuration enables precise integration into bioactive scaffolds, particularly in medicinal chemistry applications where chiral control and hydrogen-bonding capacity are critical. The molecule exhibits enhanced solubility and stability under standard handling conditions, facilitating use in peptide conjugation and macrocyclic synthesis workflows.
rel-(3R,4S)-4-Aminotetrahydrofuran-3-ol serves as a stereochemically defined building block for the synthesis of bioactive heterocycles and peptide mimetics. Its functional group pattern—bearing both hydroxyl and primary amine moieties in a constrained tetrahydrofuran ring—enables efficient derivatization via acylation, alkylation, or coupling reactions. The compound exhibits good bench stability and facilitates regioselective transformations, supporting its use in medicinal chemistry campaigns requiring chiral, polar scaffolds with predictable reactivity.
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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: