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Structure of 1784619-01-7
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6-Bromo-2,4-dichlorothieno[2,3-d]pyrimidine features a fused thienopyrimidine core with strategic halogen substitution at the 6-bromo and 2,4-positions. This electron-deficient scaffold enables direct coupling in cross-coupling reactions, serving as a key building block for functionalized heterocycles in medicinal chemistry and materials science.
6-Bromo-2,4-dichlorothieno[2,3-d]pyrimidine serves as a versatile building block for the synthesis of biologically active heterocycles, enabling efficient Suzuki-Miyaura and Buchwald-Hartwig couplings due to its well-defined halogen reactivity. The molecule exhibits excellent bench stability and facilitates straightforward purification, 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: