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Structure of 35212-85-2
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Methyl 3-Aminobenzo[b]thiophene-2-carboxylate features a fused thiophene-benzene core with a strategically positioned amino group and ester functionality. This electron-rich scaffold integrates readily into heterocyclic synthesis, serving as a key intermediate for bioactive compound development. The amine moiety enables direct derivatization, while the ester group supports subsequent transformations under standard conditions.
Methyl 3-aminobenzo[b]thiophene-2-carboxylate serves as a versatile heterocyclic building block for medicinal chemistry and materials science. The ortho-amino and ester functionalities enable sequential functionalization via Suzuki-Miyaura coupling, amide formation, or electrophilic substitution. Bench-stable and readily purified by column chromatography, it functions as a key intermediate in the synthesis of bioactive scaffolds and conjugated polymers.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: