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Structure of 540516-28-7
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This bench-stable benzimidazole derivative features a brominated heterocyclic core paired with a reactive alcohol handle. The pendant hydroxymethyl group enables straightforward functionalization, while the bromine substituent supports downstream cross-coupling transformations. This compound serves as a key building block for bioactive molecule synthesis and materials development.
(5-Bromo-1H-benzo[d]imidazol-2-yl)methanol serves as a versatile building block for the synthesis of biologically relevant heterocycles, enabling efficient functionalization at the benzoimidazole core. Its pendant aldehyde functionality facilitates nucleophilic additions, reductive amination, and coupling reactions with minimal side reactivity. The molecule exhibits excellent bench stability and is readily purified by standard chromatographic methods, making it well-suited for iterative synthesis in 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-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: