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Structure of 706-06-9
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This propargylic acid features a 4-fluorophenyl group conjugated to a reactive alkyne, enabling efficient copper-catalyzed coupling reactions. The electron-withdrawing fluorine enhances electrophilicity at the β-carbon, facilitating nucleophilic addition and click chemistry applications. Designed for modular synthesis in bioconjugation and medicinal chemistry workflows.
3-(4-Fluorophenyl)prop-2-ynoic acid serves as a versatile building block for the synthesis of functionalized arylalkynes and heterocyclic scaffolds. Its conjugated alkyne-carboxylic acid motif enables efficient coupling reactions, including Sonogashira and click chemistry protocols. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for medicinal chemistry and process development workflows.
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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: