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Structure of 898566-17-1
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This thiophene derivative features a 4-fluorophenyl group and a 5-iodo-2-methylphenylmethyl substituent, enabling efficient coupling in cross-coupling reactions. The electron-deficient thiophene core enhances reactivity in palladium-catalyzed transformations, while the iodine handle facilitates selective functionalization. Designed for synthetic precision in pharmaceutical and materials chemistry applications.
2-(4-Fluorophenyl)-5-[(5-iodo-2-methylphenyl)methyl]thiophene serves as a versatile building block for Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. The iodine substituent provides high reactivity under palladium catalysis, while the thiophene core offers stability and compatibility with diverse functional groups. Its bench-stable nature and straightforward purification facilitate integration into complex synthetic sequences for pharmaceutical and materials applications.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: