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*For research and further manufacturing use only, not for direct human use.
Structure of 56198-37-9
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tert-Butyl 5-iodopentanoate features a reactive iodide handle at the terminal position, enabling efficient late-stage functionalization in synthetic workflows. The tert-butyl ester group provides enhanced stability and ease of handling, while the aliphatic chain supports compatibility with transition-metal-catalyzed coupling reactions. This reagent serves as a valuable building block for constructing complex molecular architectures under standard conditions.
tert-Butyl 5-iodopentanoate serves as a versatile iodinated building block for transition-metal-catalyzed coupling reactions, particularly in Pd-mediated cross-couplings and cyclization processes. The iodo group exhibits high reactivity with palladium catalysts under standard conditions, enabling efficient C–C bond formation. Its tert-butyl ester functionality provides excellent bench stability and facilitates straightforward deprotection to the corresponding carboxylic acid. The molecule’s linear alkyl chain supports incorporation into diverse heterocyclic and macrocyclic scaffolds, offering practical utility in medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS06
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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-P405-P501
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Lot numbers can be found on the outside label of a product: