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Structure of 26226-72-2
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Ethyl 4-(2-chloroacetamido)benzoate features a strategically positioned chloroacetamido group that enhances reactivity in amide coupling workflows. This electron-deficient aromatic ester integrates readily into peptide synthesis and medicinal chemistry scaffolds, offering reliable stability under standard conditions.
Ethyl 4-(2-chloroacetamido)benzoate serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted benzamide derivatives. The chloroacetamido group facilitates nucleophilic displacement reactions, while the ester functionality supports selective transformations under mild conditions. Its bench-stable nature and compatibility with common coupling protocols make it ideal for constructing pharmacophores in API development.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: