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Structure of 441715-30-6
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5-Fluoro-1-methyl-1H-indole-3-carbaldehyde features a fluorinated indole core with a methyl group at the nitrogen and an aldehyde function at the 3-position. This electron-deficient scaffold integrates readily into synthetic routes for pharmaceutical intermediates, offering enhanced metabolic stability and tunable polarity.
5-Fluoro-1-methyl-1H-indole-3-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds via standard coupling and functional group transformation protocols. The aldehyde functionality facilitates efficient derivatization, while the 5-fluoro and 1-methyl substituents enhance metabolic stability and modulate electronic properties. Bench-stable and compatible with common purification methods, it functions reliably in multistep syntheses targeting bioactive molecules.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H318
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: