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Structure of 1415638-13-9
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(5-Bromo-1-methyl-1H-pyrazol-4-yl)methanol features a brominated pyrazole core with a pendant hydroxymethyl group, enabling direct functionalization in late-stage diversification. This bench-stable reagent integrates readily into synthetic sequences requiring electrophilic or coupling-compatible heterocyclic scaffolds.
(5-Bromo-1-methyl-1H-pyrazol-4-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrazole-based scaffolds. The bromo group facilitates palladium-catalyzed cross-coupling reactions, while the primary alcohol offers a handle for derivatization or protection. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for modular synthesis of bioactive compounds.
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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: