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Structure of 150637-97-1
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N-(2-Chloro-3-methoxyphenyl)acetamide features a chlorinated aromatic core paired with a methoxy substituent, delivering enhanced electron-withdrawing character and improved solubility in polar organic media. This scaffold integrates readily into pharmaceutical intermediates and functional materials, offering stable performance under standard reaction conditions.
N-(2-Chloro-3-methoxyphenyl)acetamide serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted aniline derivatives via facile amide hydrolysis or reductive cleavage. Its ortho-chloro and meta-methoxy substitution pattern provides predictable regiochemical control in subsequent coupling reactions, while the acetamide group offers excellent bench stability and compatibility with diverse reaction conditions.
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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: