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*For research and further manufacturing use only, not for direct human use.
Structure of 109113-72-6
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2-(Chloromethyl)-4-methylquinazoline features a reactive chloromethyl group positioned for efficient functionalization, enabling direct coupling in synthetic workflows. The quinazoline core provides a rigid, electron-deficient scaffold ideal for medicinal chemistry applications. This compound offers bench-stable handling and compatibility with diverse reaction conditions.
2-(Chloromethyl)-4-methylquinazoline serves as a versatile electrophilic building block for C–H functionalization and nucleophilic substitution reactions. The chloromethyl group enables efficient derivatization with amines, thiols, and other nucleophiles under mild conditions, facilitating the construction of diverse quinazoline-based scaffolds. Its bench-stable nature and compatibility with common protecting groups make it well-suited for iterative synthesis in medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: