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Structure of 703-98-0
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This hydroxy-methoxyacetophenone features a strategically positioned phenolic hydroxyl and methoxy group that enhance solubility and reactivity in polar media. The ortho-hydroxyl enables intramolecular hydrogen bonding, stabilizing reactive intermediates during synthetic transformations. Its bench-stable nature supports reliable use in multistep organic synthesis and natural product derivatization.
1-(2-Hydroxy-3-methoxyphenyl)ethanone serves as a versatile building block in synthetic organic chemistry, enabling efficient access to bioactive phenolic ketones and heterocyclic scaffolds. Its ortho-hydroxyl and meta-methoxy functionalities provide orthogonal reactivity for coupling, derivatization, and metal complexation. The compound exhibits bench stability, moderate solubility in common organic solvents, and facilitates straightforward purification via recrystallization or chromatography—making it well-suited for medicinal chemistry campaigns and natural product synthesis.
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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-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: