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Structure of 1134327-93-7
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This bromopyrimidine-acetic acid derivative features a reactive bromine at the 5-position of a pyrimidine ring, enabling efficient cross-coupling transformations. The carboxylic acid group provides a versatile handle for conjugation and derivatization under standard conditions. Designed for synthetic versatility in medicinal chemistry and materials science applications.
2-(5-Bromopyrimidin-2-yl)acetic acid serves as a versatile building block for the synthesis of pyrimidine-based pharmaceuticals and agrochemicals. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid group facilitates derivatization via amide or ester formation. Its bench-stable nature and compatibility with common protecting group strategies make it a practical reagent 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-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: