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Structure of 15308-01-7
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This chlorinated acetamide features a phenyl-substituted acetyl core paired with a 2,6-dichlorophenyl moiety, delivering enhanced stability and selective reactivity. The ortho-chlorine substitution pattern imparts steric and electronic control, enabling precise coupling in synthetic pathways. Designed for robust performance under standard conditions, this compound serves as a key intermediate in agrochemical and pharmaceutical synthesis.
2-Chloro-N-(2,6-dichlorophenyl)-N-phenylacetamide serves as a versatile building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds through standard amide coupling and cyclization protocols. Its ortho-chlorinated aryl groups enhance metabolic stability and provide favorable electronic properties for downstream functionalization. The compound exhibits good bench stability, facilitates straightforward purification, and demonstrates broad compatibility with common reaction conditions 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: