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Structure of 68432-92-8
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Methyl 3-(cyanomethyl)benzoate features a strategically positioned cyano group adjacent to a benzoate ester, enabling direct functionalization in synthetic sequences. This electron-deficient aryl system supports efficient coupling reactions and serves as a key intermediate in the construction of bioactive heterocycles. The methyl ester moiety provides a handle for selective derivatization under mild conditions.
Methyl 3-(cyanomethyl)benzoate serves as a versatile synthetic intermediate for constructing benzoyl-containing heterocycles and bioactive scaffolds. The nitrile group enables facile functionalization via hydrolysis, reduction, or nucleophilic addition, while the ester moiety supports standard transformations such as Grignard additions and reductions. Its bench-stable nature and compatibility with diverse reaction conditions make it a practical choice for medicinal chemistry campaigns 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 : 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: