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Structure of 89555-39-5
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Methyl 1-bromo-2-naphthoate features a bromine atom at the 1-position of the naphthalene core, enabling direct functionalization in cross-coupling reactions. The ester group provides solubility in common organic solvents and serves as a handle for subsequent derivatization. This compound offers high reactivity and stability under standard bench conditions.
Methyl 1-bromo-2-naphthoate serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromo functionality. The naphthoate ester moiety provides compatibility with standard deprotection and functionalization protocols, while the molecule exhibits good bench stability and ease of purification. It functions reliably in the construction of biaryl scaffolds and complex heterocycles relevant to pharmaceutical and materials synthesis.
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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: