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Structure of 85216-74-6
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tert-Butyl 11-bromoundecanoate features a brominated aliphatic chain terminating in a stable tert-butyl ester, enabling direct functionalization at the ω-position. This bifunctional handle facilitates coupling reactions under mild conditions, delivering robust access to long-chain building blocks for polymer synthesis and chemical biology applications.
tert-Butyl 11-bromoundecanoate serves as a versatile bromoalkyl building block for late-stage functionalization and chain extension in synthetic organic chemistry. Its terminal bromide enables palladium-catalyzed cross-coupling reactions, while the tert-butyl ester offers stability and convenient hydrolysis under mild conditions. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis of complex aliphatic architectures and functionalized scaffolds.
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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: