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Structure of 260430-93-1
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6-Fluoroquinoline-2-carbaldehyde features a fluorinated quinoline core with a reactive aldehyde handle at the 2-position. This electron-deficient scaffold integrates readily into heterocyclic architectures, enabling direct coupling in transition-metal-catalyzed transformations. The para-fluoro substitution enhances metabolic stability and modulates electronic properties for applications in medicinal chemistry and materials science.
6-Fluoroquinoline-2-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the quinoline core via electrophilic or nucleophilic substitution. The aldehyde group facilitates imine formation and reductive amination, while the fluorine substituent enhances metabolic stability and modulates electronic properties. Its bench-stable nature and compatibility with standard coupling reactions make it well-suited for constructing complex heterocyclic scaffolds in 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352
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Lot numbers can be found on the outside label of a product: