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Structure of 25245-29-8
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5-Iodo-1,2,3-trimethoxybenzene features three methoxy groups positioned ortho to one another, creating a highly electron-rich aromatic core. The iodine substituent at the 5-position enables efficient cross-coupling reactions under standard conditions. This compound serves as a stable, bench-ready building block for synthesizing complex polyfunctionalized arenes in medicinal chemistry and materials science applications.
5-Iodo-1,2,3-trimethoxybenzene serves as a versatile building block in cross-coupling chemistry, enabling efficient Suzuki-Miyaura and Stille reactions due to its stable iodide functionality and orthogonal methoxy protection. The trimethoxy substitution pattern enhances solubility and facilitates downstream functionalization in complex molecule synthesis. Its bench-stable nature and predictable reactivity make it ideal for iterative coupling strategies in medicinal chemistry and materials science applications.
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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-H317-H319-H335
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Precautionary Statements : P261-P264-P271-P272-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: