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Structure of 95-88-5
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4-Chlororesorcinol features a vicinal trihydroxy arrangement with a chlorine substituent at the para position, delivering enhanced electrophilicity and stability under standard bench conditions. This electron-deficient phenolic scaffold integrates readily into synthetic routes requiring selective functionalization or as a building block for bioactive heterocycles.
4-Chlororesorcinol serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted phenolic scaffolds. Its ortho-dihydroxy functionality supports directed metalation and selective functionalization, while the chlorine substituent facilitates palladium-catalyzed coupling reactions. The compound exhibits excellent bench stability and compatibility with common protecting group strategies, making it well-suited for multi-step synthesis of bioactive molecules and heterocyclic systems.
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GHS Pictogram :
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GHS No : GHS05,GHS07,GHS09
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Signal Word : Danger
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H317-H318-H401-H411
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Precautionary Statements : P261-P264-P270-P272-P273-P280-P302+P352-P362-P391-P501
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Lot numbers can be found on the outside label of a product: