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Structure of 1799610-89-1
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5-Bromo-4-chloro-6-iodothieno[2,3-d]pyrimidine features a trihalogenated heterocyclic core enabling precise diversification in cross-coupling workflows. The strategic placement of bromo, chloro, and iodo substituents supports sequential functionalization, while the electron-deficient thienopyrimidine scaffold enhances reactivity in Pd-catalyzed transformations. This compound serves as a key building block for advanced pharmaceutical intermediates and materials with tailored electronic properties.
5-Bromo-4-chloro-6-iodothieno[2,3-d]pyrimidine serves as a versatile multi-heteroatom building block for the synthesis of advanced heterocyclic scaffolds. Its orthogonal halogenation pattern enables sequential cross-coupling reactions under palladium catalysis, facilitating precise diversification at multiple positions. The compound exhibits excellent bench stability and compatibility with standard Suzuki, Stille, and Negishi coupling conditions, making it ideal for medicinal chemistry campaigns and API intermediate development.
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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: