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Structure of 37470-58-9
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Ethyl 3-bromo-4-hydroxybenzoate features a bromine substituent at the meta position relative to a hydroxyl group on a benzoate scaffold, enabling selective functionalization in synthetic sequences. The ethyl ester moiety enhances solubility and reactivity in cross-coupling reactions, while the phenolic hydroxyl supports hydrogen bonding and further derivatization. This compound serves as a key intermediate in pharmaceutical and agrochemical synthesis.
Ethyl 3-bromo-4-hydroxybenzoate serves as a versatile building block for the synthesis of substituted aromatic systems, enabling direct functionalization at the bromo and hydroxyl positions. Its stability under standard reaction conditions facilitates coupling reactions, including Suzuki and Stille couplings, while the phenolic hydroxyl group permits selective derivatization or protection. The molecule functions effectively in the construction of bioactive heterocycles and pharmaceutical intermediates, offering predictable reactivity and straightforward purification.
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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: