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Structure of 1522778-35-3
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Methyl 5-bromo-3-chloro-2-methylbenzoate features a sterically hindered aromatic core with complementary halogenation at the 5-bromo and 3-chloro positions, enabling selective cross-coupling reactions. The methyl ester group enhances solubility in organic solvents and facilitates downstream derivatization. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and functionalized aryl scaffolds.
Methyl 5-bromo-3-chloro-2-methylbenzoate serves as a versatile building block for the synthesis of substituted aromatic scaffolds, enabling sequential functionalization via palladium-catalyzed cross-coupling reactions. The ortho-methyl group enhances regioselectivity in electrophilic substitution, while the bromo and chloro substituents provide complementary sites for selective transformations. Its bench-stable nature and compatibility with standard purification protocols make it ideal for iterative synthesis in medicinal chemistry and materials science applications.
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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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: