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Structure of 57556-31-7
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Methyl 4-hydroxy-2-methylbenzoate features a phenolic hydroxyl group flanked by a methyl substituent and an ester moiety, enabling selective derivatization in synthetic sequences. This ortho-substituted scaffold offers enhanced stability under standard conditions while maintaining reactivity for coupling reactions. The molecule integrates readily into complex architectures requiring polar yet lipophilic functional handles.
Methyl 4-hydroxy-2-methylbenzoate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted phenolic scaffolds. The molecule combines a phenolic hydroxyl group with an ester functionality, allowing for selective derivatization via etherification, acylation, or metal-catalyzed coupling reactions. Its bench-stable nature and compatibility with common protecting group strategies facilitate use in multi-step synthesis, particularly in the construction of bioactive heterocycles and pharmaceutical intermediates.
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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: