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Structure of 1346541-53-4
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(5-Bromo-2-methylpyridin-3-yl)methanol features a pyridine core bearing bromo and methyl substituents at meta and ortho positions relative to the methanol group, delivering enhanced electrophilicity and stability. This bench-stable reagent integrates readily into cross-coupling and functionalization workflows, enabling efficient access to complex heterocyclic architectures in medicinal chemistry and materials synthesis.
(5-Bromo-2-methylpyridin-3-yl)methanol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient late-stage functionalization via Suzuki-Miyaura and Buchwald-Hartwig coupling reactions. The pendant alcohol group facilitates derivatization through etherification or oxidation to the aldehyde, while the bromo and methyl substituents offer orthogonal reactivity for sequential transformations. Bench-stable and amenable to purification by flash chromatography, it functions reliably in multi-step syntheses requiring regioselective heterocycle functionalization.
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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: