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Structure of 1667-01-2
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2',4',6'-Trimethylacetophenone features a sterically hindered acetyl group flanked by three methyl substituents, enhancing its stability and directing electrophilic substitution reactions. This electron-rich aryl ketone serves as a key building block in synthetic organic chemistry, particularly for constructing complex aromatic systems under mild conditions.
2',4',6'-Trimethylacetophenone serves as a versatile building block in synthetic organic chemistry, leveraging its sterically hindered aryl ketone functionality for controlled electrophilic transformations. The methyl substituents enhance bench stability and facilitate purification by reducing side reactivity. It functions effectively in Friedel-Crafts acylations, Grignard additions, and as a precursor in heterocyclic scaffold construction, particularly in the synthesis of substituted benzophenones and biologically relevant aromatic systems.
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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: