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Structure of 88139-91-7
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5-Bromo-2-(hydroxymethyl)pyridine features a pyridine ring functionalized with a bromo group at the 5-position and a hydroxymethyl substituent at the 2-position, enabling dual reactivity. This combination facilitates efficient coupling reactions in medicinal chemistry and materials synthesis. The hydroxymethyl group offers a handle for derivatization while maintaining compatibility with standard synthetic protocols.
5-Bromo-2-(hydroxymethyl)pyridine serves as a versatile building block for heterocyclic synthesis, enabling efficient functionalization at the pyridine ring and hydroxymethyl side chain. Its bromo group facilitates Suzuki-Miyaura and Stille couplings, while the primary alcohol supports oxidation, protection, or direct derivatization. The compound exhibits good bench stability and compatibility with standard purification methods, making it well-suited for medicinal chemistry campaigns and process development.
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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: