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Structure of 5043-29-8
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Methyl 4-bromo-2-naphthoate features a brominated naphthalene core with a methyl ester group, offering a versatile handle for further functionalization. This bench-stable compound integrates readily into cross-coupling reactions and serves as a key intermediate in the synthesis of complex polycyclic architectures.
Methyl 4-bromo-2-naphthoate serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions for the construction of biaryl scaffolds. The bromine substituent provides high reactivity in Suzuki, Stille, and Negishi couplings, while the ester group offers compatibility with subsequent transformations. Its bench-stable crystalline form facilitates handling and purification, making it ideal for medicinal chemistry campaigns and process development requiring reliable functional group presentation.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: