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Structure of 22536-64-7
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2-Chloro-4-methoxy-6-methylpyrimidine features a strategically positioned chloro group and methoxy substituent on a pyrimidine core, enabling selective functionalization in medicinal chemistry. The methyl group enhances lipophilicity while maintaining synthetic tractability under standard conditions. This scaffold serves as a key building block for kinase inhibitors and agrochemical intermediates.
2-Chloro-4-methoxy-6-methylpyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its chloro group facilitates nucleophilic substitution reactions, while the methoxy and methyl substituents provide orthogonal functional handles for further derivatization. The compound exhibits good bench stability and is compatible with standard coupling protocols, making it valuable for the synthesis of 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: