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Structure of 65868-63-5
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tert-Butyl 6-bromohexanoate features a brominated aliphatic chain tethered to a robust tert-butyl ester group, enabling seamless incorporation into cross-coupling reactions. The pendant bromide serves as a high-reactivity handle for palladium-catalyzed transformations, while the ester moiety offers stability and ease of manipulation under standard bench conditions.
tert-Butyl 6-bromohexanoate serves as a versatile bromoester building block for nucleophilic substitution and transition-metal-catalyzed coupling reactions. Its tert-butyl ester group provides excellent stability and ease of removal under mild acidic conditions, while the terminal bromide enables efficient functionalization via Stille, Suzuki-Miyaura, or Negishi couplings. The aliphatic chain offers flexibility in constructing diverse alkylated scaffolds relevant to medicinal chemistry and polymer synthesis.
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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-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: