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Structure of 2314-37-6
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3-Iodo-4-methoxybenzaldehyde features a methoxy group and iodine substituent positioned ortho to the aldehyde, creating a sterically accessible, electron-rich platform for cross-coupling. This bench-stable reagent integrates readily into Suzuki-Miyaura and Stille reactions, enabling efficient construction of complex aryl architectures with high functional group tolerance.
3-Iodo-4-methoxybenzaldehyde serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions such as Suzuki and Stille couplings. The aldehyde group provides a handle for reductive amination or Wittig-type transformations, while the iodide offers high reactivity in transition-metal-mediated functionalizations. Its methoxy substituent enhances solubility and modulates electronic properties, supporting efficient synthesis of complex aromatic scaffolds with predictable regiochemistry.
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GHS Pictogram :
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GHS No : GHS06,GHS09
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H400
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Precautionary Statements : P264-P270-P273-P330-P391-P405-P501
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Lot numbers can be found on the outside label of a product: