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Structure of 5900-59-4
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2-Amino-4-chlorobenzamide features a strategically positioned amino group and chloro substituent on the benzamide scaffold, enabling selective coupling reactions in medicinal chemistry. This bench-stable derivative integrates readily into heterocyclic systems and serves as a key intermediate for bioactive molecule synthesis under standard conditions.
2-Amino-4-chlorobenzamide serves as a versatile building block in medicinal chemistry, enabling the construction of diverse heterocyclic scaffolds and pharmaceutical intermediates. Its amine and amide functionalities offer orthogonal reactivity for coupling reactions and derivatization, while the chloro group provides a handle for palladium-catalyzed transformations. Bench-stable and readily purified by recrystallization, it functions effectively in standard synthetic workflows for API development.
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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: