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Structure of 56035-64-4
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2,4-Dichloro-6-methylpyrimidine-5-carbonitrile features a pyrimidine core bearing chlorine atoms at positions 2 and 4, a methyl group at 6, and a carbonitrile at 5. This electron-deficient heterocycle serves as a key scaffold in medicinal chemistry, enabling efficient coupling reactions and facilitating the construction of complex nitrogen-containing frameworks under mild conditions.
2,4-Dichloro-6-methylpyrimidine-5-carbonitrile serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrimidines via nucleophilic displacement and cross-coupling reactions. Its dual chloro groups and electron-deficient carbonitrile facilitate selective functionalization, while the methyl substituent enhances stability and solubility. This compound is particularly valuable for constructing pharmaceutically relevant scaffolds with high regiocontrol and operational robustness under standard synthetic conditions.
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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: