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Structure of 79387-71-6
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(5-Bromothien-2-yl)methanol features a brominated thiophene ring with a pendant hydroxymethyl group, enabling direct functionalization in cross-coupling and derivatization workflows. This bench-stable reagent integrates readily into complex molecular architectures where halogenated heterocycles serve as key scaffolds.
(5-Bromothien-2-yl)methanol serves as a versatile building block in synthetic organic chemistry, enabling efficient functionalization of thiophene scaffolds. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the pendant alcohol group offers orthogonal reactivity for derivatization or protection. The compound exhibits good bench stability and is readily purified by distillation or column chromatography, making it well-suited for use in medicinal chemistry and materials science applications.
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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: