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Structure of 7202-43-9
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(R)-Tetrahydrofuran-2-yl-methylamine delivers a chiral, bench-stable scaffold for asymmetric synthesis. The tetrahydrofuran ring imparts conformational rigidity, while the primary amine enables straightforward derivatization. This configuration enhances stereocontrol in catalytic transformations and supports efficient incorporation into bioactive molecules.
(R)-Tetrahydrofuran-2-yl-methylamine serves as a chiral building block for medicinal chemistry and catalytic synthesis, offering high enantiomeric purity and stability under standard reaction conditions. Its functionality enables efficient incorporation into bioactive scaffolds via amine coupling, reductive amination, or cyclization protocols. The tetrahydrofuran ring provides conformational rigidity and favorable lipophilicity, enhancing metabolic stability in lead optimization.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Warning
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UN#: 2943
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226-H315-H319-H335
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: