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Structure of 33172-56-4
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5-Bromo-2-hydroxy-3-methylbenzaldehyde features a brominated aromatic core with strategically positioned hydroxyl and methyl groups, enabling selective functionalization in synthetic routes. The aldehyde moiety provides a reactive handle for coupling reactions under mild conditions. This compound exhibits enhanced solubility in polar organic solvents and stability during storage, facilitating use in pharmaceutical intermediates and agrochemical synthesis.
5-Bromo-2-hydroxy-3-methylbenzaldehyde serves as a versatile building block in medicinal chemistry and synthetic organic research. Its ortho-hydroxyl and aldehyde functionalities enable sequential transformations, including Suzuki-Miyaura coupling and oxidation to carboxylic acids. The bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the methyl group provides steric and electronic modulation. This compound exhibits bench stability and compatibility with standard purification protocols, making it suitable for multi-step synthesis of complex heterocycles and bioactive scaffolds.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: