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Structure of 36748-88-6
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3-Iodobenzo[b]thiophene is a bench-stable heterocyclic iodide featuring a fused benzothiophene core with a strategically positioned iodine atom. This electrophilic handle enables direct coupling in palladium-catalyzed cross-coupling reactions, facilitating the construction of complex biaryl architectures. The electron-deficient thiophene ring enhances reactivity in transition metal-mediated transformations while maintaining compatibility with diverse functional groups.
3-Iodobenzo[b]thiophene serves as a versatile building block in cross-coupling chemistry, enabling efficient construction of biaryl and heteroaryl architectures. The iodine substituent facilitates reliable palladium-catalyzed coupling reactions, including Suzuki, Stille, and Negishi transformations, with high functional group tolerance. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for synthetic workflows targeting complex pharmaceutical scaffolds and advanced materials.
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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
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Precautionary Statements : P261-P280-P304+P340
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Lot numbers can be found on the outside label of a product: