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Structure of 1031927-03-3
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Methyl 2-bromo-5-cyanobenzoate features a bromine atom at the ortho position and a cyano group at the para position relative to the ester, delivering high reactivity in palladium-catalyzed cross-coupling reactions. The electron-deficient aromatic ring enhances electrophilicity, enabling efficient functionalization under mild conditions. This bench-stable derivative serves as a key intermediate in the synthesis of complex heterocycles and bioactive molecules.
Methyl 2-bromo-5-cyanobenzoate serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromo group. The nitrile and ester functionalities provide orthogonal handles for further derivatization, including hydrolysis, reduction, or nucleophilic addition. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient synthesis of complex heterocyclic scaffolds and functionalized aromatic systems.
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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: