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Structure of 953039-15-1
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2-Chloro-7-methoxyquinazoline features a chlorine atom at the 2-position and a methoxy group at the 7-position, conferring enhanced electrophilicity and solubility. This electron-deficient scaffold integrates readily into kinase inhibitor scaffolds and serves as a key intermediate in medicinal chemistry campaigns targeting receptor tyrosine kinases.
2-Chloro-7-methoxyquinazoline serves as a versatile building block in medicinal chemistry, enabling efficient construction of quinazoline-based scaffolds through nucleophilic substitution. The chloro group at C2 facilitates reliable coupling with amines and other nucleophiles under mild conditions, while the 7-methoxy substituent enhances solubility and modulates electronic properties. Its bench-stable nature and straightforward purification make it ideal for high-throughput synthesis and process 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: