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Structure of 1136-86-3
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3',4',5'-Trimethoxyacetophenone features a highly electron-rich aromatic ring stabilized by three methoxy groups, enabling efficient coupling in cross-coupling reactions. The acetyl moiety provides a reactive carbonyl for nucleophilic addition or reduction. Bench-stable and moisture-tolerant, it integrates seamlessly into complex synthesis workflows.
3',4',5'-Trimethoxyacetophenone serves as a versatile building block in medicinal chemistry and natural product synthesis, offering high functional group tolerance and bench stability. Its three methoxy groups enhance solubility and electron-donating character, facilitating electrophilic substitution and transition-metal-catalyzed coupling reactions. The acetyl functionality enables facile transformations including aldol condensations, reductions, and nucleophilic additions, making it a practical scaffold for constructing complex aromatic architectures.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: