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Structure of 65766-32-7
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6-Chloro-N-methylpyrimidin-4-amine features a chlorinated pyrimidine core with a methylamino substituent at the 4-position, delivering enhanced electron-withdrawing character and improved metabolic stability. This configuration enables efficient incorporation into pharmaceutical scaffolds, particularly in kinase inhibitors and antiviral agents, where halogen bonding and targeted polarity are critical for binding affinity. The compound exhibits excellent solubility in common organic solvents and stable handling under standard laboratory conditions.
6-Chloro-N-methylpyrimidin-4-amine 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 N-methylamino functionality provides a handle for further derivatization. The compound exhibits good bench stability and compatibility with standard coupling protocols, making it well-suited for modular synthesis of bioactive molecules and API intermediates.
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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-H317-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P272-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: