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Structure of 230955-75-6
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4-Chloro-7-methoxyquinazolin-6-yl acetate features a quinazoline core functionalized with chlorine and methoxy groups at the 4- and 7-positions, respectively, and an acetate ester at the 6-position. This configuration enables direct incorporation into kinase inhibitor scaffolds and facilitates downstream derivatization under mild conditions. The acetate moiety enhances solubility and stability in organic media while allowing for selective deprotection during synthetic sequences.
4-Chloro-7-methoxyquinazolin-6-yl acetate serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The acetate group provides enhanced bench stability and facilitates selective deprotection under mild conditions, while the 4-chloro and 7-methoxy substituents offer orthogonal reactivity for further diversification. This compound functions as a key scaffold for quinazoline-based 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-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: