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Structure of 1187836-86-7
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This boronate moiety integrates readily into Suzuki-Miyaura coupling reactions, offering enhanced reactivity under mild conditions. The para-nitro group facilitates efficient cross-coupling with arylboranes, enabling rapid access to functionalized heterocycles in synthetic workflows.
(2-Bromo-5-methylthiazol-4-yl)methanol serves as a versatile building block for thiazole-based heterocycles, enabling efficient functionalization via nucleophilic substitution and cross-coupling reactions. Its bromo group facilitates palladium-catalyzed transformations, while the pendant alcohol supports derivatization or protection strategies. The molecule exhibits bench stability and compatibility with standard synthetic workflows, making it suitable for medicinal chemistry campaigns and API intermediate development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: