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Structure of 38480-94-3
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1-(2,3-Dimethoxyphenyl)ethan-1-one features a benzene ring bearing two methoxy groups in ortho positions, conferring enhanced solubility and electronic modulation. This electron-rich aryl ketone integrates readily into synthetic sequences requiring steric and electronic control. The acetyl side chain enables direct functionalization or conjugation, making it valuable for medicinal chemistry and materials synthesis under standard conditions.
1-(2,3-Dimethoxyphenyl)ethan-1-one serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of biologically relevant scaffolds. Its ortho-dimethoxyaryl moiety exhibits favorable stability and compatibility with standard coupling reactions, facilitating C–C bond formation under mild conditions. The ketone functionality provides a reliable handle for nucleophilic additions, reductions, or enolization processes, supporting diverse downstream transformations. This compound functions effectively in multi-step syntheses requiring bench-stable, functionalized aryl ketones.
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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 : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: