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Structure of 69363-85-5
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Methyl 4-aminothiophene-3-carboxylate features a thiophene core with strategically positioned amino and ester functionalities, enabling integration into diverse heterocyclic scaffolds. The electron-rich thiophene ring enhances reactivity in transition-metal-catalyzed couplings, while the bench-stable amino group facilitates downstream derivatization. This compound serves as a key building block for bioactive molecule synthesis.
Methyl 4-aminothiophene-3-carboxylate serves as a versatile scaffold for the synthesis of biologically relevant thiophene-based heterocycles. The amino group enables direct functionalization via coupling reactions, while the ester moiety supports selective reduction or hydrolysis to access carboxylic acid derivatives. Its stability under standard reaction conditions and compatibility with diverse transformations make it a practical building block in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H320
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Precautionary Statements : P264-P305+P351+P338
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Lot numbers can be found on the outside label of a product: