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Structure of 1804402-93-4
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2-Bromo-5-(trifluoromethoxy)benzonitrile features a trifluoromethoxy group that enhances electron-withdrawal and metabolic stability, while the bromine and nitrile functionalities enable efficient cross-coupling reactions. This aromatic building block integrates readily into complex molecular architectures under standard conditions.
2-Bromo-5-(trifluoromethoxy)benzonitrile serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo and nitrile functionalities. The trifluoromethoxy group enhances metabolic stability and lipophilicity, while the aryl bromide facilitates efficient C–C bond formation under standard conditions. Its bench-stable nature and compatibility with diverse reaction environments make it ideal for constructing complex heterocyclic scaffolds and functionalized aromatic systems in API development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 3439
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302+H312-H315-H319-H331-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: