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Structure of 2040-05-3
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1-(2,6-Dichlorophenyl)ethanone features a benzoyl core substituted with two chlorine atoms at the 2- and 6-positions, imparting enhanced electrophilicity and stability. This electron-deficient aryl ketone integrates readily into C–C bond-forming reactions, serving as a key building block in synthetic routes to pharmaceutical intermediates and agrochemicals under standard conditions.
1-(2,6-Dichlorophenyl)ethanone serves as a versatile building block in medicinal chemistry, enabling efficient construction of biologically relevant aryl ketones. Its stability under standard reaction conditions and compatibility with common functional groups facilitate downstream transformations such as nucleophilic additions, reductions, and coupling reactions. The ortho-dichloro substitution pattern enhances metabolic stability and modulates lipophilicity, making it a practical scaffold for lead optimization in API development.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: