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Structure of 348-62-9
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4-Chloro-2-fluorophenol features a fluorine atom at the ortho position relative to the hydroxyl group, enhancing its electron-withdrawing character and metabolic stability. This substitution pattern imparts favorable reactivity in electrophilic aromatic substitution and facilitates coupling reactions under mild conditions. The compound serves as a key intermediate in agrochemical and pharmaceutical synthesis due to its balanced polarity and structural rigidity.
4-Chloro-2-fluorophenol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the phenolic OH and ortho-position via electrophilic substitution or transition-metal-catalyzed coupling. Its halogenated aryl scaffold offers excellent compatibility with Suzuki, Stille, and Buchwald-Hartwig reactions, facilitating rapid access to complex heterocycles and bioactive intermediates. The compound exhibits robust bench stability and straightforward purification, making it ideal for high-throughput synthesis and process 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
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Lot numbers can be found on the outside label of a product: