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Structure of 52959-28-1
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Dimethyl 4,6-dihydroxyisophthalate features two hydroxyl groups flanking a methyl ester-substituted aromatic core, enabling selective derivatization in polymer synthesis and bioconjugation. The ortho-hydroxy arrangement enhances chelation potential while the bench-stable esters tolerate standard reaction conditions. This bifunctional scaffold integrates readily into functional materials requiring polar, reactive sites.
Dimethyl 4,6-dihydroxyisophthalate serves as a versatile diol-containing aromatic building block for the synthesis of functionalized polyesters and heterocyclic scaffolds. Its two phenolic hydroxyl groups enable selective protection, derivatization, and metal coordination, while the ester functionalities support transesterification and amidation reactions. The molecule exhibits good bench stability and facilitates purification via recrystallization, making it well-suited for iterative synthetic sequences in materials chemistry and medicinal compound development.
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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: