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Structure of 4670-10-4
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This 2-(3,5-dimethoxyphenyl)acetic acid features a phenyl core with two methoxy groups in the meta and para positions relative to the acetic acid side chain. The electron-rich aromatic ring enhances reactivity in coupling reactions, while the carboxylic acid group enables direct functionalization or salt formation. Bench-stable and moisture-tolerant, it serves as a robust building block for pharmaceutical intermediates and bioactive molecule synthesis.
2-(3,5-Dimethoxyphenyl)acetic acid serves as a versatile building block for the synthesis of bioactive molecules, particularly in medicinal chemistry and agrochemical development. Its ortho-dimethoxyaryl moiety provides enhanced metabolic stability and lipophilicity modulation. The carboxylic acid functional group enables straightforward derivatization via amide, ester, or acyl chloride formation, facilitating integration into complex scaffolds. Bench-stable and readily purified by recrystallization, it functions reliably in standard coupling protocols and multistep syntheses.
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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
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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: