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Structure of 55876-84-1
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Methyl 5-(bromomethyl)picolinate features a bromomethyl group appended to the pyridine ring, enabling direct functionalization at the C5 position. This electrophilic handle facilitates efficient coupling reactions in synthetic workflows, particularly in the construction of complex heterocycles and bioconjugates. The methyl ester provides compatibility with standard reduction and amidation protocols.
Methyl 5-(bromomethyl)picolinate serves as a versatile building block for constructing pyridine-based heterocycles and bioactive scaffolds. The bromomethyl group enables efficient nucleophilic substitution, facilitating C–C and C–heteroatom bond formation under mild conditions. Its stability under standard bench handling and compatibility with diverse functional groups make it ideal for iterative synthesis in medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: