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Structure of 888-79-9
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4-Amino-N-(2-chlorophenyl)benzamide features a planar, electron-rich aromatic core with a strategically positioned para-amino group and ortho-chlorinated phenyl substituent. This combination enhances solubility in polar organic solvents while maintaining stability under standard bench conditions. The molecule integrates readily into heterocyclic scaffolds and serves as a key intermediate in the synthesis of bioactive compounds targeting kinase pathways.
4-Amino-N-(2-chlorophenyl)benzamide serves as a versatile building block in medicinal chemistry, enabling the construction of biologically relevant scaffolds through standard amide coupling and electrophilic substitution reactions. The ortho-chlorophenyl group enhances metabolic stability and provides a handle for further functionalization, while the aniline functionality offers excellent compatibility with diverse synthetic transformations. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step synthesis workflows.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: