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Structure of 2649788-79-2
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tert-Butyl (4-bromo-3-cyano-7-fluorobenzo[b]thiophen-2-yl)carbamate features a sterically hindered tert-butyl carbamate protecting group paired with electron-deficient aryl halide and nitrile functionalities. This combination enables direct coupling in Pd-catalyzed cross-coupling reactions, offering robust stability under standard conditions. The fluorine substituent enhances metabolic resistance and modulates electronic properties for downstream functionalization in medicinal chemistry applications.
tert-Butyl (4-bromo-3-cyano-7-fluorobenzo[b]thiophen-2-yl)carbamate serves as a versatile building block for the synthesis of fluorinated benzo[b]thiophene scaffolds. The molecule combines bromo, cyano, and fluoro substituents with a bench-stable carbamate group, enabling orthogonal functionalization in late-stage diversification. It facilitates palladium-catalyzed cross-coupling reactions, supports nucleophilic substitution at the bromo site, and maintains compatibility with standard protecting group strategies in medicinal chemistry workflows.
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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
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: