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Structure of 1455091-10-7
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Methyl 4-hydroxy-7-phenoxyisoquinoline-3-carboxylate features a fused heterocyclic core with a phenolic hydroxyl and phenoxy substituent, enabling versatile conjugation in bioactive molecule design. The ester functionality offers tunable reactivity under standard conditions, while the electron-rich isoquinoline scaffold supports efficient coupling reactions. This compound serves as a strategic intermediate for medicinal chemistry applications requiring rigid, planar architectures with enhanced solubility profiles.
Methyl 4-hydroxy-7-phenoxyisoquinoline-3-carboxylate serves as a versatile building block for isoquinoline-based scaffolds, enabling direct functionalization at the C4 hydroxyl and C7 phenoxy positions. Its methyl ester group facilitates downstream derivatization via hydrolysis or nucleophilic substitution, while the phenoxy moiety provides enhanced solubility and stability under standard synthetic conditions. This compound functions effectively in cross-coupling reactions and heterocycle elaboration, supporting efficient access to biologically relevant isoquinoline architectures in medicinal chemistry and materials science applications.
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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: