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Structure of 62484-31-5
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2,4-Dichloro-7-methoxyquinazoline features a sterically accessible quinazoline core with electron-withdrawing chloro groups at positions 2 and 4, paired with a methoxy substituent at C7. This combination enhances electrophilicity for nucleophilic substitution and improves solubility in polar organic media. The compound serves as a key scaffold in kinase inhibitor development and is compatible with standard coupling protocols under mild conditions.
2,4-Dichloro-7-methoxyquinazoline serves as a versatile building block in medicinal chemistry, enabling efficient construction of quinazoline-based scaffolds. The dichloro substitution pattern facilitates sequential nucleophilic aromatic substitution, allowing selective introduction of diverse amine and heterocyclic moieties. Its methoxy group enhances solubility and modulates electronic properties, while the compound exhibits excellent bench stability and ease of purification—key advantages for high-throughput synthesis and process development.
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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: