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Structure of 55860-22-5
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2-Chloro-N-(2-methoxyphenyl)acetamide features a chlorinated acetyl group linked to a methoxy-substituted phenyl ring, delivering enhanced stability and tunable reactivity. This scaffold integrates electron-donating and halogen functionalities, enabling efficient coupling in synthetic transformations. The molecule exhibits favorable solubility in common organic solvents and maintains integrity under standard bench conditions.
2-Chloro-N-(2-methoxyphenyl)acetamide serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted anilines and heterocyclic scaffolds. Its chloroacetamide functionality facilitates nucleophilic substitution and cyclization reactions under mild conditions, while the ortho-methoxyphenyl group provides steric and electronic modulation. The compound exhibits good bench stability and is readily purified by flash chromatography, making it well-suited for iterative synthesis workflows in API development.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: