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Structure of 233775-30-9
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6-Amino-1-methyl-1,2,3,4-tetrahydroquinolin-2-one features a fused heterocyclic core with a strategically positioned amino group and methyl substituent, enabling direct incorporation into bioactive scaffolds. This bench-stable compound serves as a key building block for pharmaceutical intermediates, particularly in the development of kinase inhibitors and CNS-targeted agents, where its electron-rich amine facilitates downstream functionalization under mild conditions.
6-Amino-1-methyl-1,2,3,4-tetrahydroquinolin-2-one serves as a versatile scaffold in medicinal chemistry, enabling efficient access to substituted quinolinone derivatives. The amino and carbonyl functionalities provide orthogonal reactivity for downstream modifications, including acylation, alkylation, and transition-metal-catalyzed coupling reactions. Its bench-stable nature and compatibility with common purification methods facilitate integration into multi-step synthetic sequences for API development.
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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: