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Structure of 17849-38-6
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2-Chlorobenzyl alcohol offers a reactive benzyl handle bearing an ortho-chloro substituent, enhancing electrophilic character and directing effects in subsequent transformations. This bench-stable, moisture-tolerant reagent integrates readily into synthetic sequences requiring selective functionalization or coupling reactions under standard conditions.
2-Chlorobenzyl alcohol serves as a versatile building block in medicinal chemistry and process synthesis, enabling efficient introduction of both aryl and functionalized alkyl moieties. Its benzylic alcohol functionality undergoes reliable oxidation to the aldehyde or carboxylic acid, while the ortho-chloro group provides a handle for palladium-catalyzed cross-coupling reactions. The compound exhibits good bench stability and is compatible with standard purification methods, facilitating integration into multi-step syntheses of heterocyclic scaffolds and API intermediates.
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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 : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: