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Structure of 130365-87-6
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1-(2-Bromoethyl)-4-(trifluoromethyl)benzene features a bromoethyl side chain appended to a trifluoromethyl-substituted benzene ring, enabling efficient coupling in cross-coupling reactions. The electron-deficient aryl group enhances reactivity in palladium-catalyzed transformations, while the terminal bromide serves as a reliable handle for further functionalization. This structure combines stability with synthetic versatility for advanced molecular architectures.
1-(2-Bromoethyl)-4-(trifluoromethyl)benzene serves as a versatile bifunctional building block in synthetic organic chemistry, enabling efficient construction of pharmacophoric scaffolds. The bromoethyl moiety facilitates nucleophilic substitution reactions, while the trifluoromethyl group imparts enhanced metabolic stability and lipophilicity. This compound exhibits excellent bench stability and compatibility with standard coupling protocols, making it well-suited for applications in medicinal chemistry and materials science.
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GHS No : GHS07,GHS09
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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-H319-H411
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Precautionary Statements : P264-P270-P273-P280-P305+P351+P338-P391-P501
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Lot numbers can be found on the outside label of a product: