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Structure of 159768-57-7
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5-Amino-1H-indole-3-carbonitrile features a conjugated indole core bearing an electron-rich amino group at C5 and a strongly electron-withdrawing nitrile at C3, enabling diverse synthetic transformations. This scaffold integrates readily into bioactive heterocycles and serves as a key intermediate in medicinal chemistry campaigns targeting kinase inhibitors and antitumor agents.
5-Amino-1H-indole-3-carbonitrile serves as a versatile building block for heterocyclic synthesis, enabling efficient access to indole-based scaffolds through standard coupling and cyclization protocols. The molecule exhibits robust bench stability and compatibility with diverse functional groups, facilitating straightforward purification and integration into medicinal chemistry campaigns. Its dual amino and nitrile functionalities support sequential transformations in multi-step syntheses.
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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: