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Structure of 262368-30-9
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N-(4-aminophenyl)-N-methyl-2-(4-methylpiperazin-1-yl)acetamide features a conjugated aniline handle paired with a sterically hindered piperazinyl acetyl side chain, enabling efficient coupling in bioconjugation workflows. The molecule combines enhanced solubility with bench-stable reactivity under standard conditions.
N-(4-Aminophenyl)-N-methyl-2-(4-methylpiperazin-1-yl)acetamide serves as a versatile building block in medicinal chemistry, enabling the construction of diverse heterocyclic scaffolds through standard amide coupling and cyclization protocols. Its dual functionality—aromatic amine and tertiary amide—supports efficient derivatization under mild conditions, while the piperazine moiety enhances solubility and metabolic stability. The compound exhibits excellent bench stability and compatibility with common purification techniques, facilitating scalable synthesis in drug discovery workflows.
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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: