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Structure of 6621-59-6
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6-Bromohexanenitrile features a terminal nitrile group flanked by a bromine-substituted alkyl chain, enabling direct functionalization in nucleophilic substitution and cross-coupling reactions. This bifunctional scaffold supports the synthesis of complex amides, heterocycles, and bioactive intermediates under standard conditions.
6-Bromohexanenitrile serves as a versatile bifunctional building block for synthetic organic chemistry, enabling efficient access to γ- and δ-functionalized nitriles. The bromide and nitrile groups exhibit orthogonal reactivity, facilitating palladium-catalyzed cross-coupling reactions and nucleophilic transformations under mild conditions. Its bench-stable nature and compatibility with diverse functional groups support scalable synthesis of complex intermediates, including heterocyclic scaffolds and bioactive molecule precursors.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: