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Structure of 62208-67-7
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3-Amino-1-benzofuran-2-carbonitrile features a fused benzofuran scaffold bearing an electron-rich amino group and a reactive nitrile moiety. This combination enables direct incorporation into heterocyclic architectures, facilitating rapid access to bioactive scaffolds in medicinal chemistry. The compound exhibits excellent stability under standard bench conditions and demonstrates favorable solubility in common organic solvents for synthetic manipulation.
3-Amino-1-benzofuran-2-carbonitrile serves as a versatile building block for heterocyclic synthesis, enabling efficient access to fused polycyclic scaffolds via C–H functionalization and palladium-catalyzed coupling reactions. The amino and nitrile groups offer orthogonal reactivity, facilitating derivatization through amidation, cyclization, or electrophilic substitution. Bench-stable and readily purified by recrystallization, it functions effectively in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
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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: