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Structure of 128833-03-4
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Diethyl 3-bromobenzylphosphonate features a brominated benzyl group flanked by two ethoxy phosphonate arms, enabling direct incorporation into C–C bond-forming reactions. This bench-stable reagent delivers high functional group tolerance and facilitates efficient coupling with nucleophiles under mild conditions.
Diethyl 3-bromobenzylphosphonate serves as a versatile building block for the synthesis of phosphonate-containing aromatic compounds. It enables efficient P–C bond formation in Suzuki-Miyaura and Negishi couplings, and its bromine functionality facilitates further functionalization via palladium-catalyzed cross-coupling reactions. The molecule exhibits good bench stability and is compatible with standard purification techniques, making it suitable for iterative synthetic sequences 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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: