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Structure of 98434-18-5
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2-Bromo-4-chlorophenyl acetate features a brominated and chlorinated phenyl core paired with a labile acetate ester, enabling selective derivatization in synthetic workflows. The electron-deficient aromatic ring enhances reactivity in nucleophilic substitution processes, while the acetate group serves as a transient handle for controlled release or further functionalization under mild conditions.
2-Bromo-4-chlorophenyl acetate serves as a versatile aryl halide building block in cross-coupling reactions, offering orthogonal reactivity between bromo and chloro substituents. Its bench-stable nature and compatibility with Pd-catalyzed coupling protocols enable efficient construction of biaryl architectures. The acetate ester group provides mild protection for phenolic functionality, facilitating selective transformations and simplifying purification. Functions reliably in standard synthetic workflows requiring controlled electrophilic reactivity.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: