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Structure of 85514-43-8
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This silane reagent features a bromoalkyl chain tethered to a bulky tert-butyl dimethylsilyl group, enabling selective functionalization under mild conditions. The silyl moiety provides robust protection for alcohols and amines, while the (5-bromopentyl)oxy handle facilitates efficient coupling reactions in synthetic sequences. Bench-stable and moisture-tolerant, it streamlines access to complex architectures in organic synthesis and materials chemistry.
[(5-Bromopentyl)oxy](tert-butyl)dimethylsilane serves as a robust silyl-protected hydroxyl synthon, enabling reliable etherification and chain extension in complex molecule synthesis. Its bromide handle facilitates nucleophilic substitution with amines, thiols, and carbon nucleophiles, while the bulky tert-butyldimethylsilyl group ensures excellent stability and selective deprotection under mild conditions. Ideal for constructing polyether scaffolds and functionalized intermediates in medicinal chemistry and natural product synthesis.
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GHS Pictogram :
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GHS No : GHS06,GHS08
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Signal Word : Danger
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UN#: 2810
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331-H341
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: