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Structure of 944060-66-6
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2-Chloro-8-methoxyquinazoline features a chlorine atom at the 2-position and a methoxy group at the 8-position, conferring enhanced electrophilicity and solubility. This scaffold integrates readily into medicinal chemistry libraries, serving as a key intermediate for kinase inhibitors and targeted therapeutics.
2-Chloro-8-methoxyquinazoline serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive C2-chloro group. The 8-methoxy substituent enhances solubility and modulates electronic properties, while the quinazoline core provides a stable scaffold for targeted functionalization. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient synthesis of biologically active 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-H320-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: