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Structure of 886500-41-0
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4-Chloro-2,6-difluorobenzonitrile features a trifunctional aromatic core with electron-withdrawing nitrile and halogen substituents. This bench-stable scaffold enables direct incorporation into pharmaceutical intermediates, offering enhanced reactivity in cross-coupling and nucleophilic substitution processes.
4-Chloro-2,6-difluorobenzonitrile serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of fluorinated heterocycles and substituted biaryl systems. Its orthogonal reactivity profile—combining electrophilic substitution compatibility with stable nitrile and halogen functionalities—facilitates downstream functionalization via Pd-catalyzed cross-coupling, nucleophilic aromatic substitution, and directed ortho-metalation. Bench-stable and readily purified by recrystallization, it supports scalable synthesis of complex scaffolds with enhanced metabolic stability and targeted physicochemical properties.
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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 : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: