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Structure of 136333-97-6
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Methyl 4-(2-bromoethyl)benzoate features a bromoethyl chain appended to the para position of a methyl benzoate scaffold. This electrophilic handle enables efficient coupling in nucleophilic substitution reactions, particularly in bioconjugation and polymer functionalization workflows. The compound exhibits stability under standard bench conditions and facilitates site-specific modification in complex molecular architectures.
Methyl 4-(2-bromoethyl)benzoate serves as a versatile building block for C–C and C–heteroatom bond formation, enabling efficient functionalization of aromatic systems. The bromoethyl side chain facilitates nucleophilic substitution reactions with amines, thiols, and azide derivatives, while the ester group remains stable under standard reaction conditions. Its bench-stable nature and compatibility with diverse coupling protocols make it ideal for constructing complex scaffolds in medicinal chemistry and materials synthesis.
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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: