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Structure of 113100-86-0
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Methyl 4-(3-bromopropyl)benzoate features a brominated aliphatic chain appended to a para-substituted benzoate ester. This structure enables site-specific conjugation in synthetic organic chemistry, particularly in bioconjugation and polymer functionalization workflows. The pendant bromide serves as a reactive handle for nucleophilic substitution under mild conditions.
Methyl 4-(3-bromopropyl)benzoate serves as a versatile building block for the synthesis of functionalized aromatic compounds. The bromoalkyl chain enables efficient copper-catalyzed coupling reactions and facilitates nucleophilic substitution, while the ester group offers compatibility with standard reduction and amidation protocols. Bench-stable and readily purified by column chromatography, it supports scalable access to diverse heterocyclic systems and bioactive scaffolds in medicinal chemistry workflows.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: