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Structure of 39503-52-1
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Methyl 5-bromo-2-hydroxy-4-methoxybenzoate features a brominated aromatic core with strategically positioned hydroxyl and methoxy groups, enabling selective functionalization in synthetic sequences. The ester moiety supports downstream derivatization, while the electron-withdrawing bromine enhances reactivity in cross-coupling processes. This compound exhibits bench-stable handling characteristics and compatibility with standard reaction conditions.
Methyl 5-bromo-2-hydroxy-4-methoxybenzoate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted phenolic scaffolds. The molecule combines a bromo group for late-stage functionalization via cross-coupling, a hydroxyl moiety for derivatization or protection, and a methoxy group that enhances solubility and modulates electronic properties. Its bench-stable nature and compatibility with standard reaction conditions facilitate purification and integration into multi-step syntheses of bioactive compounds.
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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: