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Structure of 19432-69-0
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Methyl 5-methylthiophene-2-carboxylate features a thiophene core with strategically positioned methyl and ester groups, enhancing solubility and stability in organic synthesis. This electron-rich heterocycle serves as a key building block for pharmaceutical intermediates and functional materials, enabling efficient coupling reactions under standard conditions.
Methyl 5-methylthiophene-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted thiophene scaffolds relevant to medicinal chemistry and materials science. The methyl ester group facilitates downstream transformations such as hydrolysis or reduction, while the 5-methylthio substituent provides a handle for selective functionalization via oxidation or cross-coupling. Bench-stable and compatible with standard reaction conditions, it functions as a reliable intermediate in multi-step syntheses.
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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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: