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Structure of 99580-50-4
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2-Amino-4-hydroxythiophene-3-carbonitrile features a fused thiophene core functionalized with amino, hydroxyl, and nitrile groups, enabling versatile integration into heterocyclic scaffolds. The electron-rich aromatic system supports efficient coupling reactions, while the hydroxyl group offers potential for derivatization or metal coordination. This bench-stable compound serves as a key intermediate in the synthesis of bioactive molecules and advanced materials.
2-Amino-4-hydroxythiophene-3-carbonitrile serves as a versatile heterocyclic building block in medicinal chemistry, enabling the construction of bioactive scaffolds through well-established functional group transformations. Its amino and hydroxyl groups offer orthogonal reactivity for derivatization, while the carbonitrile moiety supports nucleophilic addition and cyclization reactions. The compound exhibits bench stability and facilitates efficient purification, making it suitable for scalable synthesis 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-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: