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Structure of 116632-42-9
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2-Chloro-1-iodo-4-methylbenzene features a strategically positioned iodine atom enabling efficient cross-coupling reactions, while the chloro and methyl groups provide orthogonal reactivity and steric modulation. This aryl halide integrates seamlessly into transition-metal-catalyzed transformations under standard conditions.
2-Chloro-1-iodo-4-methylbenzene serves as a versatile diaryl building block for palladium-catalyzed cross-coupling reactions. The ortho-chloro and iodo substituents enable sequential functionalization, with the iodo group offering high reactivity in Suzuki, Stille, and Negishi couplings. The methyl group provides steric and electronic modulation, enhancing stability and solubility. Bench-stable and readily purified by column chromatography, it facilitates efficient access to substituted biaryls and heterocyclic scaffolds in medicinal chemistry and materials synthesis.
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GHS Pictogram :
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GHS No : GHS05,GHS07,GHS09
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Signal Word : Danger
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UN#: 3082
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335-H411
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Precautionary Statements : P261-P264-P271-P273-P280-P302+P352-P304+P340-P362+P364-P391-P405-P501
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Lot numbers can be found on the outside label of a product: