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Structure of 18776-12-0
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α-(2-Chloroethyl)benzenemethanol features a benzyl alcohol moiety linked to a chloroethyl side chain, enabling direct functionalization in synthetic transformations. This reactive handle facilitates nucleophilic substitution and serves as a key intermediate in pharmaceutical and agrochemical synthesis. The molecule exhibits enhanced stability under standard bench conditions while maintaining high reactivity toward amines and thiols.
α-(2-Chloroethyl)benzenemethanol serves as a versatile bifunctional building block in synthetic organic chemistry, combining a benzylic alcohol with a β-chloroethyl group. This motif enables straightforward derivatization via nucleophilic substitution or elimination reactions, facilitating the construction of heterocyclic scaffolds and functionalized alkyl chains. Its bench-stable nature and compatibility with common protecting group strategies make it a practical choice for iterative synthesis workflows in medicinal chemistry 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 : H302
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Precautionary Statements : P264-P270-P301+P310-P330-P501
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Lot numbers can be found on the outside label of a product: