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Structure of 1159511-24-6
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1-(1-Methyl-1H-indazol-5-yl)ethan-1-one features a fused bicyclic indazolyl core linked to a methyl ketone group, delivering a robust scaffold for medicinal chemistry. This bench-stable compound integrates readily into synthetic routes targeting kinase inhibitors and bioactive heterocycles. The electron-deficient carbonyl enables nucleophilic addition and conjugate functionalization under mild conditions.
1-(1-Methyl-1H-indazol-5-yl)ethan-1-one serves as a versatile building block for indazolyl ketones, enabling direct functionalization at the C5 position. Its stability and compatibility with standard synthetic protocols facilitate efficient derivatization in medicinal chemistry workflows. The methyl-substituted indazole core provides a rigid, planar scaffold suitable for structure-activity studies. Functions effectively in nucleophilic additions, reductive aminations, and transition-metal-catalyzed coupling reactions, offering practical utility in the construction of heterocyclic drug candidates.
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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: