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Structure of 500563-90-6
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(2-Iodo-4-nitrophenyl)methanol features a reactive iodide and electron-deficient nitro group positioned ortho to the methanol functionality, enabling efficient coupling reactions. This combination facilitates direct C–C or C–heteroatom bond formation in transition metal-catalyzed processes. The benzylic alcohol offers synthetic versatility for derivatization under mild conditions. Bench-stable and moisture-tolerant, it serves as a reliable building block in medicinal chemistry and materials synthesis.
(2-Iodo-4-nitrophenyl)methanol serves as a versatile building block for Suzuki-Miyaura and Sonogashira coupling reactions, enabling efficient construction of biaryl and arylalkynyl scaffolds. The iodide functionality provides high reactivity under palladium catalysis, while the nitro group offers orthogonal handle for subsequent reduction or functionalization. Bench-stable and readily purified by flash chromatography, it facilitates reliable access to complex heterocyclic and pharmaceutical intermediates.
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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: