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Structure of 54125-61-0
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Methyl 2-methyl-1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate features a fused bicyclic core with a methyl-substituted ketone and ester functionality, offering enhanced stability and solubility in polar organic solvents. This scaffold serves as a key intermediate in the synthesis of complex heterocycles and bioactive molecules, particularly in medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
Methyl 2-methyl-1-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylate serves as a versatile scaffold for constructing substituted tetralin derivatives. Its fused bicyclic structure provides rigidity and defined stereochemistry, enabling efficient functionalization at the C2 position. The ester group facilitates downstream transformations such as hydrolysis, reduction, or cross-coupling, while the ketone supports enolate chemistry and nucleophilic addition reactions. Bench-stable and readily purified by column chromatography, it functions effectively in synthetic routes toward bioactive heterocycles and pharmaceutical intermediates.
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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: