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Structure of 4142-98-7
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Ethyl 3,5-dihydroxybenzoate features two hydroxyl groups at the meta positions relative to the ester, enabling enhanced solubility and reactivity in polar solvents. This configuration supports selective derivatization in synthetic routes requiring controlled polarity. The compound serves as a key intermediate for bioactive molecule scaffolds, particularly in polyphenolic and antioxidant analog development.
Ethyl 3,5-dihydroxybenzoate serves as a versatile dihydroxy-substituted aromatic building block for medicinal chemistry and materials synthesis. Its two phenolic hydroxyl groups enable orthogonal functionalization, facilitating selective derivatization or protection strategies. The ester functionality supports downstream transformations such as hydrolysis or coupling reactions, while the compound exhibits good bench stability and ease of purification—ideal for use in multi-step syntheses of bioactive scaffolds and functional polymers.
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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: