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Structure of 848841-54-3
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6-Iodoquinazoline serves as a key electrophilic scaffold in transition-metal-catalyzed cross-coupling reactions. The iodine substituent enables efficient Pd- or Ni-mediated functionalization, facilitating the construction of complex quinazoline derivatives. This bench-stable compound integrates readily into pharmaceutical and agrochemical synthesis workflows.
6-Iodoquinazoline serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions for the construction of biaryl and heteroaryl scaffolds. Its iodine substituent provides high reactivity in standard Suzuki, Stille, and Negishi couplings, while the quinazoline core offers excellent stability and compatibility with diverse functional groups. This compound facilitates efficient synthesis of kinase inhibitors and other bioactive molecules, offering predictable reactivity and straightforward purification.
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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: