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Structure of 19112-35-7
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Ethyl (2-chlorobenzoyl)acetate serves as a versatile synthon in heterocyclic synthesis, enabling efficient construction of substituted benzimidazoles and quinolines via condensation and cyclization protocols. The ortho-chloro substituent enhances electrophilic reactivity while maintaining bench stability, facilitating straightforward purification and compatibility with standard coupling reactions. Its dual carbonyl functionality supports diverse transformations, including enolate-mediated alkylation and Michael additions, making it a reliable building block for medicinal chemistry and process development workflows.
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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: