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Structure of 1378387-81-5
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This fluorenone-based ketone features a brominated, difluorinated aryl core paired with a reactive chloroacetyl group. The electron-deficient fluorene scaffold enhances stability and facilitates downstream functionalization. This compound serves as a key intermediate in the synthesis of advanced organic materials and pharmaceuticals requiring precise steric and electronic control.
1-(7-Bromo-9,9-difluoro-9H-fluoren-2-yl)-2-chloroethanone serves as a versatile building block for C–C and C–heteroatom bond formation in synthetic organic chemistry. The fluorenyl scaffold offers enhanced stability and orthogonal reactivity, while the α-chloroketone functionality enables facile nucleophilic substitution and enolate-mediated coupling reactions. Its bench-stable nature and compatibility with standard purification methods make it suitable for multi-step synthesis of complex molecular architectures.
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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
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: