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Structure of 27913-96-8
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This bench-stable aldehyde features a sulfonamide-embedded thiomorpholine ring, delivering enhanced solubility and stability. The electron-deficient aromatic core enables efficient coupling in amide bond formation, while the dioxidothiomorpholino moiety acts as a polar handle for conjugation.
4-(1,1-Dioxidothiomorpholino)benzaldehyde serves as a versatile building block for the synthesis of sulfonamide-containing aromatic scaffolds. The aldehyde functionality enables direct coupling in reductive amination and Wittig-type transformations, while the 1,1-dioxidothiomorpholine group imparts high solubility and metabolic stability. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient access to complex heterocyclic systems in medicinal chemistry campaigns.
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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: