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Structure of 877131-92-5
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This acetonitrile derivative features a brominated trifluoromethylphenyl moiety, offering enhanced electron-withdrawing character and improved stability. The nitrile group enables direct functionalization in cross-coupling reactions, while the bromine atom serves as a versatile handle for palladium-catalyzed transformations. This compound integrates seamlessly into synthetic routes requiring halogenated aromatic building blocks with tunable electronic properties.
2-(4-Bromo-2-(trifluoromethyl)phenyl)acetonitrile serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo and nitrile functionalities. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the acetonitrile moiety provides a handle for further functionalization. Bench-stable and readily purified by recrystallization, it functions effectively in Suzuki-Miyaura, Negishi, and Sonogashira coupling protocols.
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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: