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Structure of 14028-68-3
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Ethyl 2-(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)acetate features a tetrahydroisoquinoline core with strategically positioned dimethoxy groups enhancing electron density and solubility. This scaffold integrates readily into bioactive molecule synthesis, offering a stable, moisture-tolerant intermediate for medicinal chemistry campaigns.
Ethyl 2-(6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)acetate serves as a versatile building block for the synthesis of tetrahydroisoquinoline-based scaffolds. The dimethoxy substitution pattern enhances solubility and modulates electronic properties, while the ethyl acetate moiety enables facile functionalization via hydrolysis or nucleophilic displacement. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient access to bioactive molecules in medicinal chemistry campaigns.
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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: