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Structure of 170456-80-1
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3-Iodo-1-tosyl-1H-indole features a tosyl group at the nitrogen and an iodine substituent at the 3-position of the indole core, enabling efficient cross-coupling reactions. The electron-deficient aromatic system enhances reactivity in palladium-catalyzed transformations, while the bench-stable nature simplifies handling. This compound serves as a key building block for synthesizing complex heterocyclic architectures in medicinal chemistry and materials science.
3-Iodo-1-tosyl-1H-indole serves as a versatile building block for C3-functionalized indole scaffolds in medicinal chemistry and materials science. The tosyl group enhances stability and directs electrophilic substitution, while the iodine moiety enables palladium-catalyzed cross-coupling reactions such as Suzuki, Stille, and Sonogashira couplings. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient synthesis of complex heterocyclic architectures.
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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-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: