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Structure of 35764-15-9
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2-Bromo-4-(trifluoromethyl)benzonitrile features a trifluoromethyl group and a nitrile moiety positioned meta to a bromine substituent on a benzene ring. This electron-deficient aryl halide enables efficient cross-coupling reactions, particularly in palladium-catalyzed processes. The molecule exhibits bench-stable handling characteristics and compatibility with diverse reaction conditions.
2-Bromo-4-(trifluoromethyl)benzonitrile serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions to construct biaryl and heteroaryl architectures. The nitrile group provides a handle for further functionalization, while the trifluoromethyl moiety enhances metabolic stability and lipophilicity—key attributes in medicinal chemistry. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient synthesis of complex scaffolds.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: