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Structure of 30818-28-1
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4-Chloro-2-hydroxybenzonitrile features a hydroxyl group ortho to a nitrile moiety on a chlorinated benzene ring, enabling direct functionalization in synthetic sequences. This electron-deficient aromatic scaffold facilitates nucleophilic substitution and serves as a key intermediate in agrochemical and pharmaceutical synthesis.
4-Chloro-2-hydroxybenzonitrile serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the phenolic hydroxyl and nitrile groups. Its ortho-hydroxyl and para-chloro substituents facilitate downstream coupling reactions, including Suzuki-Miyaura and nucleophilic substitution, with excellent bench stability and straightforward purification. Functions as a key intermediate in the synthesis of heterocyclic scaffolds and bioactive molecules.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: