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Structure of 4506-71-2
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Ethyl 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate features a fused heterocyclic core with a bench-stable amino group and an ester handle for downstream derivatization. The saturated thiophene ring imparts enhanced solubility and metabolic stability, enabling efficient integration into bioactive molecule scaffolds.
Ethyl 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate serves as a versatile scaffold for the synthesis of biologically active heterocycles. The molecule features a reducible thieno[3,2-b]indole core with an amino group at C2 and an ester function at C3, enabling diverse transformations including amidation, alkylation, and palladium-catalyzed cross-coupling. Its bench-stable nature and compatibility with standard synthetic protocols make it a practical building block for medicinal chemistry campaigns targeting CNS agents and kinase inhibitors.
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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: