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Structure of 1211589-41-1
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Methyl 5-bromo-2-(trifluoromethyl)isonicotinate features a trifluoromethyl group at the 2-position and a bromine atom at the 5-position of the isonicotinate scaffold, delivering enhanced electron-withdrawing character and enabling selective cross-coupling reactions. This bench-stable derivative integrates readily into synthetic sequences requiring halogen-directed functionalization.
Methyl 5-bromo-2-(trifluoromethyl)isonicotinate serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromine and trifluoromethyl functionalities. The ester group facilitates further derivatization, while the electron-deficient pyridine core enhances reactivity in nucleophilic substitution and heterocycle synthesis. Bench-stable and compatible with standard purification methods, it functions effectively in multistep synthetic sequences requiring orthogonal functional group handling.
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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: