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Structure of 50672-84-9
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4-Bromo-1-naphthaldehyde features a bromine substituent at the para position relative to the aldehyde group on a naphthalene core, delivering enhanced reactivity in cross-coupling transformations. This electron-deficient aromatic aldehyde serves as a key building block for pharmaceutical intermediates and functional materials, offering improved solubility and stability under standard reaction conditions.
4-Bromo-1-naphthaldehyde serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the aldehyde and bromine sites. Its naphthyl framework provides extended conjugation and enhanced stability for use in Suzuki-Miyaura couplings, Ullmann reactions, and Friedel-Crafts transformations. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis of biaryl scaffolds and heterocyclic intermediates relevant to 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 : 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: