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Structure of 35677-89-5
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This chiral building block features a (S)-configured benzyl carbamate tethered to a 2-oxotetrahydrofuran-3-yl moiety, offering high stereocontrol in asymmetric synthesis. The oxo group enhances reactivity for downstream functionalization, while the carbamate handle enables selective protection and cleavage under mild conditions.
(S)-Benzyl (2-oxotetrahydrofuran-3-yl)carbamate serves as a chiral building block for the synthesis of tetrahydrofuran-containing pharmaceuticals and natural products. Its functionality enables straightforward access to enantiopure heterocycles via reductive amination, nucleophilic addition, or ring-opening reactions. The carbamate group provides stability and facilitates purification, while the oxo substituent offers a handle for further functionalization. This compound is bench-stable and compatible with standard synthetic 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: