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Structure of 127437-29-0
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Diethyl 5-bromoisophthalate features a brominated aromatic core flanked by ethyl ester groups, enabling direct functionalization in cross-coupling and nucleophilic substitution reactions. The para-bromo substituent provides a reactive handle for palladium-catalyzed transformations, while the ester functionalities offer compatibility with standard organic synthesis protocols. This compound serves as a robust building block for pharmaceutical intermediates and advanced materials.
Diethyl 5-bromoisophthalate serves as a versatile building block in synthetic organic chemistry, enabling the construction of functionalized aromatic scaffolds via palladium-catalyzed cross-coupling reactions. The bromo group facilitates efficient Suzuki, Stille, and Negishi couplings, while the ester functionalities offer orthogonal handles for further derivatization. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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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: