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Structure of 79206-94-3
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4-(Furan-2-ylmethyl)thiomorpholine 1,1-dioxide features a furan-containing side chain that enhances solubility and metabolic stability. This thiomorpholine derivative integrates a polar sulfone group, enabling effective engagement in hydrogen bonding and polarity modulation within bioactive scaffolds. Its bench-stable nature supports reliable use in synthetic medicinal chemistry workflows.
4-(Furan-2-ylmethyl)thiomorpholine 1,1-dioxide serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to thiomorpholine-based scaffolds. Its furan-2-ylmethyl moiety provides a handle for further functionalization via electrophilic or transition-metal-catalyzed transformations. The sulfone group enhances solubility and metabolic stability, while the thiomorpholine core offers favorable conformational flexibility and hydrogen-bonding capacity. This compound exhibits excellent bench stability and is compatible with standard synthetic workflows, facilitating rapid exploration of structure–activity relationships in drug discovery programs.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: