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Structure of 91085-56-2
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Ethyl 3,5-dichlorobenzoate features a benzene ring bearing two chlorine substituents at the meta positions and an ester group at C-3. This electron-deficient aryl motif enables direct functionalization in cross-coupling reactions. The compound exhibits high stability under standard conditions and integrates readily into synthetic sequences requiring halogenated aromatic intermediates.
Ethyl 3,5-dichlorobenzoate serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of substituted aromatic scaffolds. Its dual chloro substituents at the meta positions provide orthogonal reactivity for subsequent functionalization via palladium-catalyzed cross-coupling or nucleophilic aromatic substitution. The ester group offers compatibility with standard reduction and derivatization protocols, facilitating access to key intermediates for pharmaceutical and agrochemical research. Bench-stable and readily purified by crystallization, it functions reliably in multi-step synthesis workflows.
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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-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: