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Structure of 131803-48-0
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6-Bromomethylnicotinic acid methyl ester features a bromomethyl group at the pyridine ring's 6-position, enabling direct functionalization in cross-coupling reactions. The methyl ester moiety enhances solubility and reactivity under standard conditions. This compound serves as a key building block for bioactive heterocycles and pharmaceutical intermediates.
6-Bromomethylnicotinic acid methyl ester serves as a versatile building block for the synthesis of functionalized heterocycles and bioactive molecules. The bromomethyl group enables efficient Suzuki, Stille, or nucleophilic substitution reactions, while the ester functionality supports further transformations such as hydrolysis or reduction. Its bench-stable nature and compatibility with standard coupling protocols make it ideal for medicinal chemistry and process development 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 : H302-H312-H315-H319-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: