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Structure of 327056-72-4
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Methyl 3-chloro-5-cyanobenzoate features a strategically positioned chloro group ortho to the ester and a cyano group para to the ester, creating a highly electron-deficient aromatic scaffold. This combination enables selective reactivity in cross-coupling processes and facilitates incorporation into complex molecular architectures under mild conditions. The compound exhibits excellent bench stability and solubility in common organic solvents, streamlining handling during synthetic workflows.
Methyl 3-chloro-5-cyanobenzoate serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted benzimidazoles and heterocyclic scaffolds via nucleophilic aromatic substitution. The ortho-chloro and meta-cyano groups provide orthogonal reactivity for sequential functionalization. Its bench-stable nature and compatibility with standard coupling conditions facilitate straightforward purification and scalability in API intermediate synthesis.
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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: