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Structure of 59599-49-4
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Methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-1-carboxylate features a fused bicyclic core with a ketone at the 5-position and an ester group at C1, enabling selective functionalization in synthetic routes. The rigid, electron-deficient framework supports efficient coupling reactions under standard conditions.
Methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-1-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized tetrahydro-naphthalene scaffolds. The ketone and ester functionalities support sequential transformations including reduction, nucleophilic addition, and coupling reactions. Its bench-stable nature and compatibility with standard purification methods facilitate integration into multi-step syntheses for medicinal chemistry and process development 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: