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Structure of 125237-08-3
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2-Bromo-3,5-dimethylphenol features a bromine substituent flanked by two methyl groups on the aromatic ring, creating a sterically hindered, electron-rich phenolic scaffold. This configuration enhances stability and facilitates selective coupling reactions in synthetic applications. The compound serves as a key intermediate in the construction of functionalized arenes and bioactive molecules.
2-Bromo-3,5-dimethylphenol serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted aromatic systems via palladium-catalyzed cross-coupling reactions. The bromine substituent facilitates reliable C–C bond formation under standard Suzuki, Stille, or Negishi conditions, while the phenolic hydroxyl group allows for orthogonal protection or derivatization. Its bench-stable nature and predictable reactivity make it suitable for iterative synthesis of complex scaffolds in medicinal chemistry and materials science applications.
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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: