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Structure of 4815-24-1
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Ethyl 2-amino-4,5-dimethylthiophene-3-carboxylate features a sterically hindered thiophene core with complementary electron-rich amine and ester functionalities. This bench-stable scaffold integrates readily into heterocyclic synthesis, enabling efficient access to functionalized thienyl building blocks for medicinal chemistry and materials applications.
Ethyl 2-amino-4,5-dimethylthiophene-3-carboxylate serves as a versatile heterocyclic building block for the synthesis of substituted thiophenes and fused polycycles. The amino and ester functionalities enable sequential transformations, including coupling reactions, cyclizations, and derivatization under standard conditions. Its bench-stable nature and compatibility with diverse reaction environments facilitate efficient access to complex scaffolds relevant in medicinal chemistry and materials science.
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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: