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Structure of 1194760-84-3
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2-Amino-5-bromo-3-methylphenol features a strategically positioned amino group adjacent to a bromine substituent, enabling selective coupling reactions. The methyl group enhances solubility and steric profile, while the phenolic hydroxyl supports hydrogen bonding in synthetic intermediates. This scaffold serves as a key building block for bioactive molecules and functional materials under standard conditions.
2-Amino-5-bromo-3-methylphenol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the amino and phenolic positions. Its bromo group facilitates palladium-catalyzed cross-coupling reactions, while the methyl and hydroxyl functionalities offer orthogonal reactivity for derivatization. The compound exhibits good bench stability and is readily purified by crystallization, supporting efficient integration into multi-step syntheses of heterocyclic scaffolds and API intermediates.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: