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Structure of 76575-71-8
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Methyl 3-amino-5-methylthiophene-2-carboxylate features a thiophene core with complementary amino and methyl substituents that enhance electron density and regioselectivity in cross-coupling reactions. The ester functionality enables straightforward derivatization, while the bench-stable, moisture-tolerant nature supports reliable handling in synthetic workflows.
Methyl 3-amino-5-methylthiophene-2-carboxylate serves as a versatile heterocyclic building block for medicinal chemistry and agrochemical synthesis. The amino and methylthio substituents enable diverse functionalization, while the ester group facilitates downstream transformations. Its bench-stable nature and compatibility with standard coupling and cyclization protocols make it well-suited for iterative synthesis of bioactive thiophene scaffolds.
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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: