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Structure of 51100-47-1
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tert-Butyl 7-bromoheptanoate features a brominated aliphatic chain tethered to a tert-butyl ester, offering a robust handle for downstream functionalization. This bench-stable reagent facilitates efficient coupling reactions in synthetic routes requiring controlled carbon–carbon bond formation.
tert-Butyl 7-bromoheptanoate serves as a versatile bromoalkyl building block for C–C bond formation via cross-coupling reactions. Its tert-butyl ester functionality provides enhanced stability and ease of purification, while the terminal bromide enables reliable Suzuki, Stille, and Negishi coupling processes. The molecule functions effectively in multi-step syntheses requiring controlled functional group introduction and orthogonal reactivity, making it well-suited for the construction of complex alkyl chains and heterocyclic scaffolds in medicinal chemistry and process R&D workflows.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 3272
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H225-H315-H319-H335
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: