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Structure of 143165-48-4
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Ethyl 2-(3-chloropropoxy)acetate features a chlorinated aliphatic chain appended to an ester-functionalized acetic acid scaffold. This electrophilic ether moiety enables efficient coupling in nucleophilic substitution reactions, particularly in the synthesis of bioactive heterocycles and pharmaceutical intermediates. The molecule exhibits good stability under standard bench conditions and facilitates straightforward derivatization.
Ethyl 2-(3-chloropropoxy)acetate serves as a versatile bifunctional building block for the synthesis of bioactive molecules and heterocyclic scaffolds. Its chloroalkoxy functionality enables efficient nucleophilic displacement reactions, while the ester group supports selective transformations under standard conditions. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic sequences in medicinal chemistry and process development workflows.
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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: