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Structure of 54357-18-5
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1-Bromo-3-methylnaphthalene features a bromine substituent at the 1-position and a methyl group at the 3-position of the naphthalene core. This electron-deficient aromatic system facilitates efficient cross-coupling reactions, particularly in palladium-catalyzed transformations. The methyl group enhances solubility and provides steric control during reaction optimization. This compound serves as a valuable building block for functionalized polycyclic scaffolds in medicinal chemistry and materials science.
1-Bromo-3-methylnaphthalene serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura and Stille couplings. The bromine atom provides high reactivity under standard conditions, while the methyl group enhances regioselectivity in electrophilic substitutions. Its bench-stable nature and compatibility with diverse functional groups make it ideal for constructing complex polycyclic architectures and advanced intermediates in 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-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: