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Structure of 956101-10-3
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2-Chloro-7-fluoroquinazoline delivers a highly reactive platform for constructing advanced heterocyclic architectures. The ortho-chloro and para-fluoro substituents enable selective coupling under mild conditions, while the electron-deficient core supports efficient integration into pharmaceutical scaffolds and functional materials.
2-Chloro-7-fluoroquinazoline serves as a versatile building block in medicinal chemistry, enabling direct functionalization at C2 and C7 positions via palladium-catalyzed cross-coupling reactions. Its dual electrophilic sites offer high reactivity in Suzuki, Stille, and Buchwald-Hartwig transformations, facilitating rapid access to substituted quinazoline scaffolds. Bench-stable and readily purified by flash chromatography, it functions efficiently in multi-step synthesis of kinase inhibitors and other bioactive heterocycles.
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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: