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Structure of 41234-43-9
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Ethyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate features a rigid, electron-rich tetrahydroisoquinoline core paired with a reactive ester handle. This scaffold integrates readily into synthetic routes for bioactive alkaloids and pharmaceutical intermediates, offering predictable cyclization behavior under mild conditions.
Ethyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient construction of isoquinoline-based scaffolds. Its carboxylate functionality facilitates direct derivatization via ester hydrolysis or reduction, while the tetrahydroisoquinoline core exhibits excellent compatibility with diverse coupling reactions and functional group interconversions. Bench-stable and readily purified by standard chromatographic methods, it functions as a key intermediate in the synthesis of bioactive molecules and heterocyclic APIs.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: