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Structure of 121553-38-6
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2-Chloro-4-cyclopropyl-6-methylpyrimidine features a sterically hindered pyrimidine core with electron-withdrawing chlorine and electron-donating methyl groups, enabling selective reactivity in cross-coupling processes. The cyclopropyl substituent enhances metabolic stability and modulates lipophilicity, making this scaffold valuable for medicinal chemistry applications.
2-Chloro-4-cyclopropyl-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 cyclopropyl and methyl substituents provide steric and electronic modulation. The compound exhibits good bench stability and compatibility with standard coupling protocols, facilitating rapid diversification in target-oriented synthesis.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: