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Structure of 2737-19-1
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This phenolic compound features a bromine substituent at the ortho position and a hydroxymethyl group at the para position relative to the phenolic OH, enabling selective functionalization in synthetic routes. The hydroxymethyl moiety offers a handle for derivatization, while the bromine serves as a reactive site for cross-coupling reactions. Bench-stable under standard conditions, it supports efficient access to complex aromatic architectures in medicinal chemistry and materials synthesis.
2-Bromo-5-(hydroxymethyl)phenol serves as a versatile building block for functionalized aromatic scaffolds, enabling efficient derivatization via Suzuki-Miyaura and Stille couplings. The bromo group provides reliable electrophilic reactivity, while the hydroxymethyl functionality offers orthogonal handles for oxidation, protection, or further substitution—facilitating access to complex phenolic architectures with high synthetic flexibility and bench stability.
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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: