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Structure of 36776-32-6
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4-(2-Hydroxyacetyl)benzonitrile features a hydroxylated acetyl group flanking a nitrile-bearing aromatic ring, enabling dual reactivity in synthetic transformations. This bench-stable scaffold integrates readily into complex molecular architectures, particularly in medicinal chemistry and materials synthesis where polar functionality and electron-withdrawing character are advantageous.
4-(2-Hydroxyacetyl)benzonitrile serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive scaffolds through condensation and cyclization reactions. The pendant hydroxyl group facilitates derivatization and enhances solubility, while the nitrile moiety supports nucleophilic addition and ring formation under mild conditions. Its bench-stable nature and compatibility with standard purification protocols make it well-suited 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 : H302-H312-H315-H319-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: