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Structure of 18362-30-6
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2-Chloro-6-hydroxybenzaldehyde features a hydroxyl group flanked by electron-withdrawing chlorine and aldehyde functionalities, enabling selective functionalization in aromatic synthesis. This ortho-directed reactivity profile supports efficient coupling processes under mild conditions.
2-Chloro-6-hydroxybenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct functionalization at the aromatic ring due to its complementary electron-withdrawing chlorine and reactive aldehyde group. The hydroxyl moiety provides a handle for derivatization or protection, while the aldehyde facilitates reductive amination, Schiff base formation, or coupling reactions. Its bench-stable nature and compatibility with standard synthetic protocols make it well-suited for modular scaffold construction in multi-step sequences.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: