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Structure of 202197-61-3
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N-(2-Aminoethyl)methanesulfonamide hydrochloride features a primary amine and sulfonamide group separated by an ethylene linker, delivering enhanced solubility and stability under standard conditions. This bifunctional scaffold enables efficient conjugation in bioconjugation workflows and serves as a key building block for targeted therapeutics.
N-(2-Aminoethyl)methanesulfonamide hydrochloride serves as a versatile bifunctional building block in medicinal chemistry, enabling efficient conjugation via its primary amine and sulfonamide groups. The hydrochloride salt enhances solubility and stability in aqueous systems, facilitating use in peptide coupling, macrocyclization, and scaffold diversification. Its well-documented compatibility with standard amide bond formation and orthogonal protection strategies makes it a practical choice for synthesizing targeted therapeutics and bioactive heterocycles.
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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: