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Structure of 100-67-4
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Potassium phenoxide serves as a potent nucleophile in organic synthesis, enabling efficient C–O and C–C bond formations under mild conditions. This bench-stable reagent features high solubility in polar aprotic solvents, facilitating reactions with electrophiles such as alkyl halides and epoxides. Its robust performance simplifies the preparation of aryl ethers and functionalized aromatics in process development workflows.
Potassium phenoxide serves as a reliable, bench-stable nucleophile in C–O and C–C bond-forming reactions. It facilitates efficient arylation processes, including Williamson ether synthesis and electrophilic aromatic substitution, with consistent yields and minimal side product formation. Its high solubility in polar aprotic solvents enables straightforward reaction setup and purification, making it well-suited for scalable laboratory synthesis and process 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 : 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: