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Structure of 5751-48-4
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2-Methyl-4H-chromen-4-one features a fused benzopyrone core with a methyl substituent at the C2 position, conferring enhanced electron density and stability. This scaffold serves as a key intermediate in synthesizing bioactive natural product analogs and functionalized heterocycles under standard conditions.
2-Methyl-4H-chromen-4-one serves as a versatile scaffold in synthetic organic chemistry, enabling efficient access to substituted coumarin derivatives. Its readily available methyl group facilitates electrophilic substitution and functionalization, while the chromenone core exhibits stability under standard reaction conditions. The compound functions as a key building block in the synthesis of natural product analogs and bioactive heterocycles, offering predictable reactivity in Pd-catalyzed cross-coupling and Michael addition processes.
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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-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: