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Structure of 54589-54-7
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Ethyl 3-(chloromethyl)benzoate features a reactive chloromethyl group flanked by an electron-rich aromatic ring and an ester functionality, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. This bench-stable reagent integrates readily into complex molecular architectures under mild conditions.
Ethyl 3-(chloromethyl)benzoate serves as a versatile synthetic intermediate, enabling efficient introduction of a reactive chloromethyl group at the meta position of a benzoate scaffold. It functions as a key building block for heterocycle construction and side-chain functionalization in medicinal chemistry workflows. The molecule exhibits good bench stability and compatibility with standard nucleophilic substitution reactions, facilitating straightforward derivatization under mild conditions.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H290-H314
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Precautionary Statements : P234-P260-P264-P280-P301+P330+P331-P304+P340-P390-P405-P406-P501
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Lot numbers can be found on the outside label of a product: