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Structure of 1301214-60-7
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This isoquinoline derivative features a conjugated carbonyl and carboxylic acid moiety, enabling direct integration into heterocyclic synthesis. The electron-deficient ring system supports transition metal-catalyzed couplings and facilitates functionalization at the 5- and 7-positions under mild conditions. Bench-stable and moisture-tolerant, it serves as a key scaffold for bioactive molecule development.
1-Oxo-1,2-dihydroisoquinoline-6-carboxylic acid serves as a versatile scaffold for heterocyclic synthesis, enabling efficient access to isoquinoline-based medicinal intermediates. Its carboxylic acid functionality facilitates direct derivatization and coupling reactions, while the ortho-quinone-like structure supports electrophilic substitution and metal-catalyzed transformations. Bench-stable and compatible with standard purification methods, it functions reliably in multi-step synthetic sequences targeting bioactive molecules.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: