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Structure of 647831-24-1
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7-Bromo-1,1,1-trifluoroheptan-2-one features a bromine-substituted alkyl chain flanked by a trifluoromethyl group and a ketone functionality. This electron-deficient carbonyl system enables efficient nucleophilic addition reactions under mild conditions. The molecule’s bench-stable nature and compatibility with common organic solvents streamline its use in synthetic workflows involving fluorinated building blocks.
7-Bromo-1,1,1-trifluoroheptan-2-one serves as a versatile building block for fluorinated carbonyl chemistry, enabling efficient synthesis of trifluoromethyl-substituted heterocycles and pharmaceutical intermediates. Its α-bromoketone functionality facilitates nucleophilic addition, enolate formation, and coupling reactions under standard conditions. The molecule exhibits good bench stability and compatibility with common protecting groups, supporting scalable transformations in medicinal chemistry and process development 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: