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Structure of 7017-48-3
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This brominated acetic acid derivative features a methoxy-substituted aryl ring, enabling efficient coupling reactions in medicinal chemistry. The para-bromo and ortho-methoxy groups provide distinct electronic and steric handles for diversification. Bench-stable and compatible with standard synthetic protocols.
2-(5-Bromo-2-methoxyphenyl)acetic acid serves as a versatile building block for the synthesis of biologically active compounds, enabling efficient incorporation of brominated aromatic and methoxy functionalities. Its stability under standard reaction conditions and compatibility with palladium-catalyzed cross-coupling reactions facilitate downstream derivatization in medicinal chemistry and process development workflows.
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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: