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Structure of 1203655-71-3
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(R)-4-(1-Aminoethyl)benzenesulfonamide hydrochloride features a chiral α-aminoethyl side chain attached to a sulfonamide-functionalized aromatic ring, delivering enhanced solubility and metabolic stability. This bench-stable derivative integrates readily into bioactive scaffolds for targeted kinase inhibition and CNS drug discovery.
(R)-4-(1-Aminoethyl)benzenesulfonamide hydrochloride serves as a chiral building block for sulfonamide-containing pharmaceutical intermediates. Its bench-stable hydrochloride salt form enables straightforward handling and purification, while the (R)-configured aminoethyl side chain provides stereochemical control in target-directed synthesis. The molecule participates reliably in standard amide coupling and nucleophilic substitution reactions, facilitating access to bioactive heterocycles and kinase inhibitor scaffolds.
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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: