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Structure of 93340-09-1
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Methyl 3-cyano-2-methylbenzoate features a conjugated nitrile group flanked by a methyl substituent and ester functionality, enabling facile integration into heterocyclic syntheses. The electron-deficient aromatic ring supports nucleophilic substitution under mild conditions, while the ester moiety offers compatibility with cross-coupling protocols. This compound serves as a key scaffold in medicinal chemistry for constructing bioactive benzimidazole and quinoline derivatives.
Methyl 3-cyano-2-methylbenzoate serves as a versatile synthetic building block for the construction of heterocyclic scaffolds and bioactive molecules. Its ortho-substituted benzoate core enables efficient functionalization via palladium-catalyzed cross-coupling, while the nitrile group facilitates nucleophilic addition and cyclization reactions. The methyl ester provides a stable handle for selective transformations, and the molecule exhibits good bench stability and ease of purification—making it well-suited for iterative synthesis 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: