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Structure of 170737-46-9
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6-Bromo-2-naphthaldehyde features a bromine substituent at the 6-position and an aldehyde group at the 2-position of the naphthalene core. This electron-deficient scaffold enables direct functionalization in transition metal-catalyzed cross-coupling reactions, offering high reactivity under standard conditions. The compound exhibits excellent stability and is readily handled in air, making it ideal for synthetic workflows requiring robust, bench-stable building blocks.
6-Bromo-2-naphthaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of biologically relevant heterocycles and functionalized naphthalene scaffolds. Its electrophilic aldehyde group facilitates nucleophilic additions and condensation reactions, while the bromine substituent supports palladium-catalyzed cross-coupling transformations. The compound exhibits good bench stability and is readily purified by recrystallization or column chromatography, making it well-suited for iterative synthesis workflows in medicinal chemistry and materials science.
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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 : H315-H319
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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: