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Structure of 149436-41-9
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N-(4-(2-Aminoacetyl)-5-methoxy-2-phenoxyphenyl)methanesulfonamide hydrochloride features a phenoxy-substituted aryl scaffold with dual polar functionalities: a methoxy group enhancing solubility and a sulfonamide moiety enabling hydrogen bonding. This bench-stable derivative integrates seamlessly into bioactive molecule scaffolds for medicinal chemistry applications.
N-(4-(2-Aminoacetyl)-5-methoxy-2-phenoxyphenyl)methanesulfonamide hydrochloride serves as a versatile intermediate in medicinal chemistry, enabling the construction of complex heterocyclic scaffolds through standard amide coupling and cyclization protocols. Its methanesulfonamide group enhances solubility and metabolic stability, while the phenolic ether and aminoacetyl functionalities support diverse downstream modifications. The hydrochloride salt ensures excellent bench stability and ease of handling in multi-step syntheses.
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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: