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Structure of 29333-41-3
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Methyl 3,5-bis(bromomethyl)benzoate features two bromomethyl groups flanking a methyl ester on a benzene ring, enabling dual functionalization in synthetic sequences. This electron-deficient aromatic scaffold facilitates nucleophilic substitution and cross-coupling reactions under standard conditions. The compound's bench-stable nature supports reliable handling in multi-step syntheses.
Methyl 3,5-bis(bromomethyl)benzoate serves as a versatile bis-electrophilic building block for the construction of symmetric and functionalized heterocyclic scaffolds. The bromomethyl groups enable efficient alkylation, Suzuki-Miyaura coupling, and nucleophilic substitution reactions under mild conditions. Its bench-stable nature and compatibility with diverse reaction environments facilitate straightforward purification and integration into multi-step synthetic sequences, making it ideal for medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: