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Structure of 1803600-05-6
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This bench-stable boronate moiety integrates readily into Suzuki-Miyaura coupling reactions, enabling efficient access to functionalized heteroaryl scaffolds. The para-nitro group enhances reactivity in cross-coupling processes, while the hydrochloride salt ensures high solubility and ease of handling under standard conditions.
(5-Bromofuran-2-yl)methanamine hydrochloride serves as a versatile building block for the synthesis of brominated heterocyclic scaffolds and functionalized furan derivatives. Its amine functionality enables straightforward coupling reactions, including reductive amination and nucleophilic substitution, while the bromo substituent facilitates further diversification via palladium-catalyzed cross-coupling. The hydrochloride salt enhances bench stability and simplifies handling and purification, making it well-suited for medicinal chemistry and process development workflows.
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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-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: