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Structure of 1011484-23-3
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6-Fluoro-3-methyl-1H-indole features a fluorinated indole core with enhanced electron deficiency at the C6 position and a methyl group at C3, enabling selective functionalization in medicinal chemistry. This bench-stable scaffold integrates readily into bioactive molecules, particularly those targeting CNS receptors and kinase pathways.
6-Fluoro-3-methyl-1H-indole serves as a valuable building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles through standard coupling and functionalization reactions. Its electron-deficient aromatic ring and strategically positioned fluorine and methyl groups offer enhanced metabolic stability and tunable electronic properties. The compound exhibits good bench stability and facilitates efficient derivatization under mild conditions, making it well-suited for modular scaffold development in API research.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: