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Structure of 35212-99-8
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Methyl 5,6-dimethoxybenzothiophene-2-carboxylate features a benzothiophene core with strategically positioned methoxy groups enhancing solubility and electronic modulation. This electron-rich scaffold integrates readily into synthetic routes for bioactive heterocycles, offering robust stability under standard conditions and facilitating efficient functionalization at the carboxylate handle.
Methyl 5,6-dimethoxybenzothiophene-2-carboxylate serves as a versatile building block in medicinal chemistry, enabling the construction of benzothiophene-based scaffolds prevalent in kinase inhibitors and CNS-targeted therapeutics. The dimethoxy substitution pattern enhances solubility and modulates electronic properties, while the ester group facilitates downstream transformations including hydrolysis, amidation, or cross-coupling reactions. Bench-stable and readily purified by column chromatography, it functions effectively in standard synthetic workflows.
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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: